Showing results 1 to 2 of 2
Title | Author(s) | Issue Date | Views | |
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A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type Journal:American Journal of Medical Genetics | 2004 | 111 | ||
Novel mutation in the gene encoding c-Abl-binding protein SH3BP2 causes cherubism Journal:American Journal of Medical Genetics | 2003 | 192 |