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pro vyhledávání: '"Véronique M. Wunderle"'
Autor:
Véronique M. Wunderle, Nicholas D. Hastie, Peter N. Goodfellow, Andreas Schedl, Ricky Critcher
Publikováno v:
Proceedings of the National Academy of Sciences. 95:10649-10654
Campomelic dysplasia (CD) is a rare, neonatal human chondrodysplasia characterized by bowing of the long bones and often associated with male-to-female sex-reversal. Patients present with either heterozygous mutations in the SOX9 gene or chromosome r
Publikováno v:
Genomics. 36(2)
The mammalian Y-linked testis determining gene, SRY, encodes a protein with a DNA binding motif known as the HMG box. A large family of genes sharing a high similarity with the SRY HMG box and named Sox (Sry-related HMG box) in mouse and SOX in human
Autor:
Richard M. Korn, Yashin Ramkissoon, Véronique M. Wunderle, Peter N. Goodfellow, Cheni Kwok, Vanessa E. King
Publikováno v:
Cell. 77:785-786