Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations (Q43801039)
Jump to navigation
Jump to search
scientific article published on October 18, 2010
Language | Label | Description | Also known as |
---|---|---|---|
English | Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations |
scientific article published on October 18, 2010 |
Statements
1 reference
Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations (English)
1 reference
S. Yano
B. Baskin
A. Bagheri
K. Moseley
A. Nishimura
N. Matsumoto
18 October 2010
1 reference
1 reference
80
1 reference
5
1 reference
466-471
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference