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Familial Simpson–Golabi–Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations

✍ Scribed by S Yano; B Baskin; A Bagheri; Y Watanabe; K Moseley; A Nishimura; N Matsumoto; PN Ray


Book ID
110889158
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
626 KB
Volume
80
Category
Article
ISSN
0009-9163

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