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Microdeletion in the SHOX 3′ region associated with skeletal phenotypes of Langer mesomelic dysplasia in a 45,X/46,X,r(X) infant and Leri–Weill dyschondrosteosis in her 46,XX mother: Implication for the SHOX enhancer

✍ Scribed by Maki Fukami; Torayuki Okuyama; Shunji Yamamori; Gen Nishimura; Tsutomu Ogata


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
192 KB
Volume
137A
Category
Article
ISSN
1552-4825

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