TY  - GEN
AU  - Chassaing,N
AU  - De Mas,P
AU  - Tauber,M
AU  - Vincent,M C
AU  - Julia,S
AU  - Bourrouillou,G
AU  - Calvas,P
AU  - Bieth,E
TI  - Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype
SN  - 1552-4825
PY  - 2005///0218
KW  - Adolescent
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 2
KW  - Cytogenetic Analysis
KW  - Female
KW  - Fibrous Dysplasia, Polyostotic
KW  - genetics
KW  - Humans
KW  - Karyotyping
KW  - Microsatellite Repeats
KW  - Pedigree
KW  - Phenotype
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/ajmg.a.30199
ER  -