DOI:
10.1055/s-00000015
European Journal of Pediatric Surgery
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References
Yano S, Baskin B, Bagheri A. et al.
Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations.
Clin Genet 2011;
80 (05) 466-471
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