✦ LIBER ✦
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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