- Titre
- Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype
- Créateurs - sans rôle
- N Chassaing - Purpan Hospital, Department of Medical Genetics, Toulouse, FranceP DE MAS - Purpan Hospital, Department of Medical Genetics, Toulouse, FranceM Tauber - Children Hospital, Department of Endocrinology, Toulouse, FranceM. C Vincent - Purpan Hospital, Department of Medical Genetics, Toulouse, FranceS Julia - Purpan Hospital, Department of Medical Genetics, Toulouse, FranceG Bourrouillou - Purpan Hospital, Department of Medical Genetics, Toulouse, FranceP Calvas - Purpan Hospital, Department of Medical Genetics, Toulouse, FranceE Bieth - Purpan Hospital, Department of Medical Genetics, Toulouse, France
- Détails de publication
- American journal of medical genetics, Vol.128A(4), pp.410-413
- Éditeur
- Wiley-Liss
- Nombre de pages
- 4
- Identifiants
- 99158854509311
- Unité académique
- Physiologie et Médecine Expérimentale du coeur et des muscles - PhyMedExp
- Langue
- English
- Type de ressource
- Journal article
Article de revue
Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype
American journal of medical genetics, Vol.128A(4), pp.410-413
01/08/2004
PMID: 15264288
Indicateurs
1 Consultations de la notice