Showing results 1 to 9 of 9
Title | Author(s) | Issue Date | Views | |
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2005 | 175 | |||
2005 | ||||
Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia Journal:American Journal of Medical Genetics | 2002 | 203 | ||
2008 | ||||
2002 | 191 | |||
Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar [5] Journal:Clinical Genetics | 2007 | |||
2009 | ||||
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 | ||
2004 | 194 |