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Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype

✍ Scribed by Chassaing, N. ;De Mas, P. ;Tauber, M. ;Vincent, M.C. ;Julia, S. ;Bourrouillou, G. ;Calvas, P. ;Bieth, E.

Publisher: John Wiley and Sons
Year: 2004
Tongue: English
Weight: 97 KB
Volume: 128A
Category: Article
ISSN: 0148-7299
DOI: 10.1002/ajmg.a.30199

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