Showing results 1 to 3 of 3
Title | Author(s) | Issue Date | |
---|---|---|---|
2008 | |||
Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar [5] Journal:Clinical Genetics | 2007 | ||
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 |