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Prader-Willi syndrome due to 15q11-q13 deletion in a girl with an inherited (13;14) Robertsonian translocation

✍ Scribed by Alliende, Angélica ;Curotto, Bianca ;Maria, Lorena Santa ;Cortés, Fanny ;Aracena, Mariana

Publisher: John Wiley and Sons
Year: 2002
Tongue: English
Weight: 57 KB
Volume: 113
Category: Article
ISSN: 0148-7299
DOI: 10.1002/ajmg.10799

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