Available Puppies

The litters in the lists of available puppies are given gratis by the ABNF.
Only there are those produced by breeders ABNF members. These lists are not exhaustive.
Puppies products must have been in accordance with the principles laid down by the ABNF, including the detection of hereditary defects.
We indicate the name of the mother, the score of the litter in the quotation grid, the number of male and female puppies available. Check that the breeder offers only puppies of this litter.
These lists are updated regularly on indications of breeders.
BHCF can not be held responsible for disputes that could occur between a breeder and the purchaser of a puppy.
No mating announced

1 litter announced

Eleveurs Géniteurs Portée
Signataire de la charte du BHCF SIRET 48811823300037
Romain & Sabrina DELEPLANQUE
9 ROUTE DE LA TORRE
24230 - VELINES
Tel : +33 5 53 22 41 08
GSM : +33 6 14 70 15 74
+33 6 21 12 83 07
Email : romain.deleplanque@orange.fr
sabrory.deleplanque@sfr.fr
Lice : MOJE LUSTRA UTEX
  • Identifiée : 250269591310194
  • née le : 05/02/2023
  • LOF 11709/1603
  • Cotation : 1pt

    QUOTATION GRID
    Please see the relevant section for the breed concerned on the site of the ABNF

  • HD-A

    Hip Dysplasia
    HD-A : No signs of hip dysplasia
    HD-B

    hips almost normal
    HD-C : Hip Dysplasia light
    HD-D : Hip Dysplasia average
    HD-E severe hip Dysplasia
    Accepted : Old name for dogs allowed to reproduce.
    in principle A or B

      DM1A-1.1 DM: Degenerative myelopathy (see FAQ)
    DM1a-1.1
    Free of degenerative myelopathy
    DM1a-1.2
    Carrier of degenerative myelopathy
    DM1a-2.2
    Sick. There is a very high probability that it will gradually paralyze. Must not reproduce.
      SDCA1-1.1

    SDCA1 Dégénérescence Spongieuse avec Ataxie Cérébelleuse
    SDCA1-1.1 : INDEMNE DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 1
    SDCA1-1.2 : PORTEUR DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 1
    SDCA1-2.2 : ATTEINT DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 1
    Voir la FAQ pour plus de renseignements

      SDCA2-1.1

    SDCA2 Dégénérescence Spongieuse avec Ataxie Cérébelleuse
    SDCA2-1.1 : INDEMNE DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 2
    SDCA2-1.2 : PORTEUR DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 2
    SDCA2-2.2 : ATTEINT DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 2
    Voir la FAQ pour plus de renseignements

     
age de cession : 8 semaines

Naissance : 20/05/2025

Effectif
total
Disponibles
MâlesFemelles
9 0 1
Etalon : SIFENG DU DOMAINE DE LA VEYSSIERE
  • LOF 10083/1205
    Livres des origines
    LOFFrance (Livre des Origines Français)
    LOSH, ALSH, RISHBelgique (Livre des Origines St Hubert), (Registre Initial St Hubert)
    NHSBPays-Bas
    SHSB, LOSSuisse
    LOLLuxembourg
    VDH ou VDH/clubAllemagne
    OZB, OEHZBAutriche
    LOI, LO, ST, LIR (titre initial)Italie
    FI, FIN, SFFinlande
    FCPRPorto-Rico
    SLR
    SKK
    LOEEspagne
    GBKGilbratar
    BEK, BEA. GR-F et GR-NGrèce
    HRCroatie
    AKCUSA (American Kennel Club)
    CYAChypre
    CLP, CSHPKRépublique Tchèque
    DKKDanemark
    ESTEstonie
    JRSerbie
    KW, PKRPologne
    LOPPortugal
    KCKCanada
    CORRoumanie
    METHongrie
    KC, KCSBGrande-Bretagne (Kennel Club Stud Book)
    IKCIrlande
    IS, ISOIslande
    MKCMalte
    SKKSuede
    UKUUkraine
    RKFRussie
    NKKNorvege
  • Cotation : 2pts

    QUOTATION GRID
    Please see the relevant section for the breed concerned on the site of the ABNF

  • HD-A

    Hip Dysplasia
    HD-A : No signs of hip dysplasia
    HD-B

    hips almost normal
    HD-C : Hip Dysplasia light
    HD-D : Hip Dysplasia average
    HD-E severe hip Dysplasia
    Accepted : Old name for dogs allowed to reproduce.
    in principle A or B

      DM1A-1.2DM: Degenerative myelopathy (see FAQ)
    DM1a-1.1
    Free of degenerative myelopathy
    DM1a-1.2
    Carrier of degenerative myelopathy
    DM1a-2.2
    Sick. There is a very high probability that it will gradually paralyze. Must not reproduce.
      SDCA1-1.1

    SDCA1 Dégénérescence Spongieuse avec Ataxie Cérébelleuse
    SDCA1-1.1 : INDEMNE DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 1
    SDCA1-1.2 : PORTEUR DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 1
    SDCA1-2.2 : ATTEINT DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 1
    Voir la FAQ pour plus de renseignements

      SDCA2-1.2

    SDCA2 Dégénérescence Spongieuse avec Ataxie Cérébelleuse
    SDCA2-1.1 : INDEMNE DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 2
    SDCA2-1.2 : PORTEUR DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 2
    SDCA2-2.2 : ATTEINT DEGENERESCENCE SPONGIEUSE ATAXIE CEREBELLEUSE TYPE 2
    Voir la FAQ pour plus de renseignements

     
Obs: Parents Sociables et très proche des Humains, enfants, Elevés en Famille, Travail en Sauvetage..
No mating announced

No litter announced

No mating announced

No litter announced

No mating announced

No litter announced

1 matting announced

Eleveurs Géniteurs Renseignements
Signataire de la charte del'ABNF
SIRET 89303629300015
ANGÉLIQUE COURAULT
28 rue des jonquilles

28190 - SEREZ
Tel : +33 6 88 96 89 56
Email : couschapendoes@aol.com
Lice : PRALINE DES OURSONS MALICIEUX
  • Identifiée : 250268732578316
  • née le : 09/04/2019
  • LOF 3292/578 <table style="font: normal .9rem serif; border: thin;" cellspacing="0"> <caption style="font: bolder 1rem;" align="center" valign="top">Livres des origines</caption> <tr><th>LOF</th><td>France (Livre des Origines Français)</td></tr> <tr><th>LOSH, ALSH, RISH</th><td>Belgique (Livre des Origines St Hubert), (Registre Initial St Hubert)</td></tr> <tr><th>NHSB</th><td>Pays-Bas</td></tr> <tr><th>SHSB, LOS</th><td>Suisse</td></tr> <tr><th>LOL</th><td>Luxembourg</td></tr> <tr><th>VDH ou VDH/<i>club</i></th><td>Allemagne</td></tr> <tr><th>OZB, OEHZB</th><td>Autriche</td></tr> <tr><th>LOI, LO, ST, LIR (titre initial)</th><td>Italie</td></tr> <tr><th>FI, FIN, SF</th><td>Finlande</td></tr> <tr><th>FCPR</th><td>Porto-Rico</td></tr> <tr><th>SLR</th><td></td></tr> <tr><th>SKK</th><td></td></tr> <tr><th>LOE</th><td>Espagne</td></tr> <tr><th>GBK</th><td>Gilbratar</td></tr> <tr><th>BEK, BEA. GR-F et GR-N</th><td>Grèce</td></tr> <tr><th>HR</th><td>Croatie</td></tr> <tr><th>AKC</th><td>USA (American Kennel Club)</td></tr> <tr><th>CYA</th><td>Chypre</td></tr> <tr><th>CLP, CSHPK</th><td>République Tchèque</td></tr> <tr><th>DKK</th><td>Danemark</td></tr> <tr><th>EST</th><td>Estonie</td></tr> <tr><th>JR</th><td>Serbie</td></tr> <tr><th>KW, PKR</th><td>Pologne</td></tr> <tr><th>LOP</th><td>Portugal</td></tr> <tr><th>KCK</th><td>Canada</td></tr> <tr><th>COR</th><td>Roumanie</td></tr> <tr><th>MET</th><td>Hongrie</td></tr> <tr><th>KC, KCSB</th><td>Grande-Bretagne (Kennel Club Stud Book)</td></tr> <tr><th>IKC</th><td>Irlande</td></tr> <tr><th>IS, ISO</th><td>Islande</td></tr> <tr><th>MKC</th><td>Malte</td></tr> <tr><th>SKK</th><td>Suede</td></tr> <tr><th>UKU</th><td>Ukraine</td></tr> <tr><th>RKF</th><td>Russie</td></tr> <tr><th>NKK</th><td>Norvege</td></tr> </table>
  • Cotation : 4pts (Recommandé) <p><strong>QUOTATION GRID</ strong> <br/>Please see the relevant section for the breed concerned on the site of the ABNF </p>
  • HD-A

    Hip Dysplasia
    HD-A : No signs of hip dysplasia
    HD-B

    hips almost normal
    HD-C : Hip Dysplasia light
    HD-D : Hip Dysplasia average
    HD-E severe hip Dysplasia
    Accepted : Old name for dogs allowed to reproduce.
    in principle A or B

      ED-0 Elbow Dysplasia
    ED-0 : Eyes for elbow dysplasia
    ED-SL : Stade limit dysplasia elbow
    ED-1 : slight elbow dysplasia
    ED-2 : average elbow dysplasia
    ED-3 : severe elbow dysplasia

      PRA-0 PRA: Progressive Retinal Atrophy
    PRA-0
    The subject does not show evidence of disease at the time of ophthalmological examination.
    PRA-1
    The subject has signs of disease on clinical examination or ERG.
    It must absolutely not reproduce.
      GPRA-1.1 PRA: Progressive Retinal Atrophy
    GPRA-1.1
    The subject is declared free to genetic testing, it carries no disease gene.
    GPRA-1.2
    the subject is diagnosed as healthy carriers of the disease through genetic testing. It will never be sick.
    GPRA-2.2
    The subject is detected homozygous carrier of the gene of the PRA. If it is not already, the subject will become BLIND
    It must absolutely not be used for breeding.
      CAT-0 Cataract
    CAT-0 Free from cataract
    CAT-1Affected by cataract
      RDYS-0

    Dysplasie de la rétine
    Voir la FAQ

     

Date de saillie : 14/09/2025

Naissance prévue le : 16/11/2025

Etalon : ROYAL BALIN'S TIBONE
  • LOF 3416/514 <table style="font: normal .9rem serif; border: thin;" cellspacing="0"> <caption style="font: bolder 1rem;" align="center" valign="top">Livres des origines</caption> <tr><th>LOF</th><td>France (Livre des Origines Français)</td></tr> <tr><th>LOSH, ALSH, RISH</th><td>Belgique (Livre des Origines St Hubert), (Registre Initial St Hubert)</td></tr> <tr><th>NHSB</th><td>Pays-Bas</td></tr> <tr><th>SHSB, LOS</th><td>Suisse</td></tr> <tr><th>LOL</th><td>Luxembourg</td></tr> <tr><th>VDH ou VDH/<i>club</i></th><td>Allemagne</td></tr> <tr><th>OZB, OEHZB</th><td>Autriche</td></tr> <tr><th>LOI, LO, ST, LIR (titre initial)</th><td>Italie</td></tr> <tr><th>FI, FIN, SF</th><td>Finlande</td></tr> <tr><th>FCPR</th><td>Porto-Rico</td></tr> <tr><th>SLR</th><td></td></tr> <tr><th>SKK</th><td></td></tr> <tr><th>LOE</th><td>Espagne</td></tr> <tr><th>GBK</th><td>Gilbratar</td></tr> <tr><th>BEK, BEA. GR-F et GR-N</th><td>Grèce</td></tr> <tr><th>HR</th><td>Croatie</td></tr> <tr><th>AKC</th><td>USA (American Kennel Club)</td></tr> <tr><th>CYA</th><td>Chypre</td></tr> <tr><th>CLP, CSHPK</th><td>République Tchèque</td></tr> <tr><th>DKK</th><td>Danemark</td></tr> <tr><th>EST</th><td>Estonie</td></tr> <tr><th>JR</th><td>Serbie</td></tr> <tr><th>KW, PKR</th><td>Pologne</td></tr> <tr><th>LOP</th><td>Portugal</td></tr> <tr><th>KCK</th><td>Canada</td></tr> <tr><th>COR</th><td>Roumanie</td></tr> <tr><th>MET</th><td>Hongrie</td></tr> <tr><th>KC, KCSB</th><td>Grande-Bretagne (Kennel Club Stud Book)</td></tr> <tr><th>IKC</th><td>Irlande</td></tr> <tr><th>IS, ISO</th><td>Islande</td></tr> <tr><th>MKC</th><td>Malte</td></tr> <tr><th>SKK</th><td>Suede</td></tr> <tr><th>UKU</th><td>Ukraine</td></tr> <tr><th>RKF</th><td>Russie</td></tr> <tr><th>NKK</th><td>Norvege</td></tr> </table>
  • Cotation : 4pts (Recommandé) <p><strong>QUOTATION GRID</ strong> <br/>Please see the relevant section for the breed concerned on the site of the ABNF </p>
  • PRA-0 <strong> PRA: Progressive Retinal Atrophy </strong> <dl><dt>PRA-0</dt><dd>The subject does not show evidence of disease at the time of ophthalmological examination.</dd><dt>PRA-1</dt><dd>The subject has signs of disease on clinical examination or ERG. <br />It must absolutely not reproduce.</dd></dl>
  • GPRA-1.2 <strong> PRA: Progressive Retinal Atrophy </strong> <dl><dt>GPRA-1.1 </dt><dd> The subject is declared free to genetic testing, it carries no disease gene. </dd><dt>GPRA-1.2 </dt><dd> the subject is diagnosed as healthy carriers of the disease through genetic testing. It will never be sick.</dd><dt>GPRA-2.2</dt><dd> The subject is detected homozygous carrier of the gene of the PRA. If it is not already, the subject will become BLIND <br /> It must absolutely not be used for breeding.</dd></dl> CAT-0 <strong> Cataract </strong> <table><tr> <th> CAT-0 </th><td> Free from cataract </td></tr><tr><th>CAT-1</th><td>Affected by cataract</td></tr></table> RDYS-0 <p>Dysplasie de la rétine<br>Voir la FAQ</p>
4 litters announced

Eleveurs Géniteurs Portée
Signataire de la charte du BHCF SIRET 53441549200014
Mme Marie Christine HURST
52 C rue de la Semm

68000 - COLMAR
Tel : +33 6 72 73 14 98
GSM : +33 6 72 73 14 98
Email : leboisdesnonnes@orange.fr
Lice : PAIVI IRWAEN DU BOIS DES NONNES
  • Identifiée : 250268501657726
  • née le : 17/01/2019
  • LOF 3278/597
  • Cotation : 4pts (Recommandé)

    QUOTATION GRID
    Please see the relevant section for the breed concerned on the site of the ABNF

  • PRA-0 PRA: Progressive Retinal Atrophy
    PRA-0
    The subject does not show evidence of disease at the time of ophthalmological examination.
    PRA-1
    The subject has signs of disease on clinical examination or ERG.
    It must absolutely not reproduce.
      GPRA-1.1 PRA: Progressive Retinal Atrophy
    GPRA-1.1
    The subject is declared free to genetic testing, it carries no disease gene.
    GPRA-1.2
    the subject is diagnosed as healthy carriers of the disease through genetic testing. It will never be sick.
    GPRA-2.2
    The subject is detected homozygous carrier of the gene of the PRA. If it is not already, the subject will become BLIND
    It must absolutely not be used for breeding.
      CAT-0 Cataract
    CAT-0 Free from cataract
    CAT-1Affected by cataract
      RDYS-0

    Dysplasie de la rétine
    Voir la FAQ

     
age de cession : 8 semaines

Naissance : 23/09/2025

Effectif
total
Disponibles
MâlesFemelles
7 3 1
Etalon : VERY CHARMING MR BOJANGLES DES UNS ET DES AUTRES
  • ROI 17/57836
    Livres des origines
    LOFFrance (Livre des Origines Français)
    LOSH, ALSH, RISHBelgique (Livre des Origines St Hubert), (Registre Initial St Hubert)
    NHSBPays-Bas
    SHSB, LOSSuisse
    LOLLuxembourg
    VDH ou VDH/clubAllemagne
    OZB, OEHZBAutriche
    LOI, LO, ST, LIR (titre initial)Italie
    FI, FIN, SFFinlande
    FCPRPorto-Rico
    SLR
    SKK
    LOEEspagne
    GBKGilbratar
    BEK, BEA. GR-F et GR-NGrèce
    HRCroatie
    AKCUSA (American Kennel Club)
    CYAChypre
    CLP, CSHPKRépublique Tchèque
    DKKDanemark
    ESTEstonie
    JRSerbie
    KW, PKRPologne
    LOPPortugal
    KCKCanada
    CORRoumanie
    METHongrie
    KC, KCSBGrande-Bretagne (Kennel Club Stud Book)
    IKCIrlande
    IS, ISOIslande
    MKCMalte
    SKKSuede
    UKUUkraine
    RKFRussie
    NKKNorvege
  • non coté (chien étranger)

    QUOTATION GRID
    Please see the relevant section for the breed concerned on the site of the ABNF

  • HD-A

    Hip Dysplasia
    HD-A : No signs of hip dysplasia
    HD-B

    hips almost normal
    HD-C : Hip Dysplasia light
    HD-D : Hip Dysplasia average
    HD-E severe hip Dysplasia
    Accepted : Old name for dogs allowed to reproduce.
    in principle A or B

      ED-0 Elbow Dysplasia
    ED-0 : Eyes for elbow dysplasia
    ED-SL : Stade limit dysplasia elbow
    ED-1 : slight elbow dysplasia
    ED-2 : average elbow dysplasia
    ED-3 : severe elbow dysplasia

      PRA-0 PRA: Progressive Retinal Atrophy
    PRA-0
    The subject does not show evidence of disease at the time of ophthalmological examination.
    PRA-1
    The subject has signs of disease on clinical examination or ERG.
    It must absolutely not reproduce.
      GPRA-1.1 PRA: Progressive Retinal Atrophy
    GPRA-1.1
    The subject is declared free to genetic testing, it carries no disease gene.
    GPRA-1.2
    the subject is diagnosed as healthy carriers of the disease through genetic testing. It will never be sick.
    GPRA-2.2
    The subject is detected homozygous carrier of the gene of the PRA. If it is not already, the subject will become BLIND
    It must absolutely not be used for breeding.
      CAT-0 Cataract
    CAT-0 Free from cataract
    CAT-1Affected by cataract
      RDYS-0

    Dysplasie de la rétine
    Voir la FAQ

     
Obs:
Signataire de la charte du BHCF SIRET 89525774900013
Mlle Marie GIRARD
Domaine des Pinchinats
Rue du Vignemale
65310 - ODOS
Tel : +33 6 03 38 29 92
GSM : +33 6 03 38 29 92
Email : mariegrd@gmail.com
Lice : NISKA DU ROYAUME DE FANELIA
  • Identifiée : 250268501252515
  • née le : 02/11/2017
  • LOF 3235/568
  • Cotation : 3pts

    QUOTATION GRID
    Please see the relevant section for the breed concerned on the site of the ABNF

  • PRA-0 PRA: Progressive Retinal Atrophy
    PRA-0
    The subject does not show evidence of disease at the time of ophthalmological examination.
    PRA-1
    The subject has signs of disease on clinical examination or ERG.
    It must absolutely not reproduce.
      GPRA-1.1 PRA: Progressive Retinal Atrophy
    GPRA-1.1
    The subject is declared free to genetic testing, it carries no disease gene.
    GPRA-1.2
    the subject is diagnosed as healthy carriers of the disease through genetic testing. It will never be sick.
    GPRA-2.2
    The subject is detected homozygous carrier of the gene of the PRA. If it is not already, the subject will become BLIND
    It must absolutely not be used for breeding.
      CAT-0 Cataract
    CAT-0 Free from cataract
    CAT-1Affected by cataract
      RDYS-0

    Dysplasie de la rétine
    Voir la FAQ

     
age de cession : 8 semaines

Naissance : 18/09/2025

Effectif
total
Disponibles
MâlesFemelles
4 1 1
Etalon : NEWTON DES FARFADETS DE LA PAGERIE
  • LOF 3187/00474
    Livres des origines
    LOFFrance (Livre des Origines Français)
    LOSH, ALSH, RISHBelgique (Livre des Origines St Hubert), (Registre Initial St Hubert)
    NHSBPays-Bas
    SHSB, LOSSuisse
    LOLLuxembourg
    VDH ou VDH/clubAllemagne
    OZB, OEHZBAutriche
    LOI, LO, ST, LIR (titre initial)Italie
    FI, FIN, SFFinlande
    FCPRPorto-Rico
    SLR
    SKK
    LOEEspagne
    GBKGilbratar
    BEK, BEA. GR-F et GR-NGrèce
    HRCroatie
    AKCUSA (American Kennel Club)
    CYAChypre
    CLP, CSHPKRépublique Tchèque
    DKKDanemark
    ESTEstonie
    JRSerbie
    KW, PKRPologne
    LOPPortugal
    KCKCanada
    CORRoumanie
    METHongrie
    KC, KCSBGrande-Bretagne (Kennel Club Stud Book)
    IKCIrlande
    IS, ISOIslande
    MKCMalte
    SKKSuede
    UKUUkraine
    RKFRussie
    NKKNorvege
  • Cotation : 3pts

    QUOTATION GRID
    Please see the relevant section for the breed concerned on the site of the ABNF

  • PRA-0 PRA: Progressive Retinal Atrophy
    PRA-0
    The subject does not show evidence of disease at the time of ophthalmological examination.
    PRA-1
    The subject has signs of disease on clinical examination or ERG.
    It must absolutely not reproduce.
      GPRA-1.1 PRA: Progressive Retinal Atrophy
    GPRA-1.1
    The subject is declared free to genetic testing, it carries no disease gene.
    GPRA-1.2
    the subject is diagnosed as healthy carriers of the disease through genetic testing. It will never be sick.
    GPRA-2.2
    The subject is detected homozygous carrier of the gene of the PRA. If it is not already, the subject will become BLIND
    It must absolutely not be used for breeding.
      CAT-0 Cataract
    CAT-0 Free from cataract
    CAT-1Affected by cataract
      RDYS-0

    Dysplasie de la rétine
    Voir la FAQ

     
Obs:
Signataire de la charte du BHCF SIRET 394944888
Mme SANDRINE LANNUZEL
34 rue saint Thudon
29490 - GUIPAVAS
Tel : +33 7 70 22 43 28
GSM : +33 7 70 22 43 28
Email : sandrine29800@gmail.com
Lice : OUPS DU ROYAUME DE FANELIA
  • Identifiée : 250268501450278
  • née le : 22/04/2018
  • LOF 3250/571
  • Cotation : 4pts (Recommandé)

    QUOTATION GRID
    Please see the relevant section for the breed concerned on the site of the ABNF

  • HD-A

    Hip Dysplasia
    HD-A : No signs of hip dysplasia
    HD-B

    hips almost normal
    HD-C : Hip Dysplasia light
    HD-D : Hip Dysplasia average
    HD-E severe hip Dysplasia
    Accepted : Old name for dogs allowed to reproduce.
    in principle A or B

      ED-0 Elbow Dysplasia
    ED-0 : Eyes for elbow dysplasia
    ED-SL : Stade limit dysplasia elbow
    ED-1 : slight elbow dysplasia
    ED-2 : average elbow dysplasia
    ED-3 : severe elbow dysplasia

      OCD-0

    Voir la FAQ

      PRA-0 PRA: Progressive Retinal Atrophy
    PRA-0
    The subject does not show evidence of disease at the time of ophthalmological examination.
    PRA-1
    The subject has signs of disease on clinical examination or ERG.
    It must absolutely not reproduce.
      GPRA-1.2 PRA: Progressive Retinal Atrophy
    GPRA-1.1
    The subject is declared free to genetic testing, it carries no disease gene.
    GPRA-1.2
    the subject is diagnosed as healthy carriers of the disease through genetic testing. It will never be sick.
    GPRA-2.2
    The subject is detected homozygous carrier of the gene of the PRA. If it is not already, the subject will become BLIND
    It must absolutely not be used for breeding.
      CAT-0 Cataract
    CAT-0 Free from cataract
    CAT-1Affected by cataract
      RDYS-0

    Dysplasie de la rétine
    Voir la FAQ

     
age de cession : 8 semaines

Naissance : 19/08/2025

Effectif
total
Disponibles
MâlesFemelles
5 0 1
Etalon : TUDY DES LOUSTICS DE PEN AR BED
  • LOF 3448/516
    Livres des origines
    LOFFrance (Livre des Origines Français)
    LOSH, ALSH, RISHBelgique (Livre des Origines St Hubert), (Registre Initial St Hubert)
    NHSBPays-Bas
    SHSB, LOSSuisse
    LOLLuxembourg
    VDH ou VDH/clubAllemagne
    OZB, OEHZBAutriche
    LOI, LO, ST, LIR (titre initial)Italie
    FI, FIN, SFFinlande
    FCPRPorto-Rico
    SLR
    SKK
    LOEEspagne
    GBKGilbratar
    BEK, BEA. GR-F et GR-NGrèce
    HRCroatie
    AKCUSA (American Kennel Club)
    CYAChypre
    CLP, CSHPKRépublique Tchèque
    DKKDanemark
    ESTEstonie
    JRSerbie
    KW, PKRPologne
    LOPPortugal
    KCKCanada
    CORRoumanie
    METHongrie
    KC, KCSBGrande-Bretagne (Kennel Club Stud Book)
    IKCIrlande
    IS, ISOIslande
    MKCMalte
    SKKSuede
    UKUUkraine
    RKFRussie
    NKKNorvege
  • Cotation : 4pts (Recommandé)

    QUOTATION GRID
    Please see the relevant section for the breed concerned on the site of the ABNF

  • HD-A

    Hip Dysplasia
    HD-A : No signs of hip dysplasia
    HD-B

    hips almost normal
    HD-C : Hip Dysplasia light
    HD-D : Hip Dysplasia average
    HD-E severe hip Dysplasia
    Accepted : Old name for dogs allowed to reproduce.
    in principle A or B

      ED-0 Elbow Dysplasia
    ED-0 : Eyes for elbow dysplasia
    ED-SL : Stade limit dysplasia elbow
    ED-1 : slight elbow dysplasia
    ED-2 : average elbow dysplasia
    ED-3 : severe elbow dysplasia

      PRA-0 PRA: Progressive Retinal Atrophy
    PRA-0
    The subject does not show evidence of disease at the time of ophthalmological examination.
    PRA-1
    The subject has signs of disease on clinical examination or ERG.
    It must absolutely not reproduce.
      GPRA-1.1 PRA: Progressive Retinal Atrophy
    GPRA-1.1
    The subject is declared free to genetic testing, it carries no disease gene.
    GPRA-1.2
    the subject is diagnosed as healthy carriers of the disease through genetic testing. It will never be sick.
    GPRA-2.2
    The subject is detected homozygous carrier of the gene of the PRA. If it is not already, the subject will become BLIND
    It must absolutely not be used for breeding.
      CAT-0 Cataract
    CAT-0 Free from cataract
    CAT-1Affected by cataract
      RDYS-0

    Dysplasie de la rétine
    Voir la FAQ

     
Obs: Belle petite portée de toutes les couleurs 1 femelle noire et blanche 1 femelle noire et grise 1 femelle marron et blanche réservée 1 mâle noir et gris 1 mâle marron réservé
Signataire de la charte du BHCF SIRET 394944888
Mme SANDRINE LANNUZEL
34 rue saint Thudon
29490 - GUIPAVAS
Tel : +33 7 70 22 43 28
GSM : +33 7 70 22 43 28
Email : sandrine29800@gmail.com
Lice : R'TEYSS DU BOSQUET DES ELFES
  • Identifiée : 250268743543131
  • née le : 08/12/2020
  • LOF 3352/588
  • Cotation : 4pts (Recommandé)

    QUOTATION GRID
    Please see the relevant section for the breed concerned on the site of the ABNF

  • HD-A

    Hip Dysplasia
    HD-A : No signs of hip dysplasia
    HD-B

    hips almost normal
    HD-C : Hip Dysplasia light
    HD-D : Hip Dysplasia average
    HD-E severe hip Dysplasia
    Accepted : Old name for dogs allowed to reproduce.
    in principle A or B

      ED-0 Elbow Dysplasia
    ED-0 : Eyes for elbow dysplasia
    ED-SL : Stade limit dysplasia elbow
    ED-1 : slight elbow dysplasia
    ED-2 : average elbow dysplasia
    ED-3 : severe elbow dysplasia

      PRA-0 PRA: Progressive Retinal Atrophy
    PRA-0
    The subject does not show evidence of disease at the time of ophthalmological examination.
    PRA-1
    The subject has signs of disease on clinical examination or ERG.
    It must absolutely not reproduce.
      GPRA-1.1 PRA: Progressive Retinal Atrophy
    GPRA-1.1
    The subject is declared free to genetic testing, it carries no disease gene.
    GPRA-1.2
    the subject is diagnosed as healthy carriers of the disease through genetic testing. It will never be sick.
    GPRA-2.2
    The subject is detected homozygous carrier of the gene of the PRA. If it is not already, the subject will become BLIND
    It must absolutely not be used for breeding.
      CAT-0 Cataract
    CAT-0 Free from cataract
    CAT-1Affected by cataract
      RDYS-0

    Dysplasie de la rétine
    Voir la FAQ

     
age de cession : 8 semaines

Naissance : 17/08/2025

Effectif
total
Disponibles
MâlesFemelles
9 3 3
Etalon : ROYAL BALIN'S THAO
  • LOF 3423/00513
    Livres des origines
    LOFFrance (Livre des Origines Français)
    LOSH, ALSH, RISHBelgique (Livre des Origines St Hubert), (Registre Initial St Hubert)
    NHSBPays-Bas
    SHSB, LOSSuisse
    LOLLuxembourg
    VDH ou VDH/clubAllemagne
    OZB, OEHZBAutriche
    LOI, LO, ST, LIR (titre initial)Italie
    FI, FIN, SFFinlande
    FCPRPorto-Rico
    SLR
    SKK
    LOEEspagne
    GBKGilbratar
    BEK, BEA. GR-F et GR-NGrèce
    HRCroatie
    AKCUSA (American Kennel Club)
    CYAChypre
    CLP, CSHPKRépublique Tchèque
    DKKDanemark
    ESTEstonie
    JRSerbie
    KW, PKRPologne
    LOPPortugal
    KCKCanada
    CORRoumanie
    METHongrie
    KC, KCSBGrande-Bretagne (Kennel Club Stud Book)
    IKCIrlande
    IS, ISOIslande
    MKCMalte
    SKKSuede
    UKUUkraine
    RKFRussie
    NKKNorvege
  • Cotation : 1pt

    QUOTATION GRID
    Please see the relevant section for the breed concerned on the site of the ABNF

  • PRA-0 PRA: Progressive Retinal Atrophy
    PRA-0
    The subject does not show evidence of disease at the time of ophthalmological examination.
    PRA-1
    The subject has signs of disease on clinical examination or ERG.
    It must absolutely not reproduce.
      GPRA-1.2 PRA: Progressive Retinal Atrophy
    GPRA-1.1
    The subject is declared free to genetic testing, it carries no disease gene.
    GPRA-1.2
    the subject is diagnosed as healthy carriers of the disease through genetic testing. It will never be sick.
    GPRA-2.2
    The subject is detected homozygous carrier of the gene of the PRA. If it is not already, the subject will become BLIND
    It must absolutely not be used for breeding.
      CAT-0 Cataract
    CAT-0 Free from cataract
    CAT-1Affected by cataract
      RDYS-0

    Dysplasie de la rétine
    Voir la FAQ

     
Obs: Belle portée de 9 chiots 4 femelles noires et grises 1 femelle noire et blanche 3 mâles noirs et gris 1 mâle noir et blanc
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