Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14
| Data(s) |
2008
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|---|---|
| Resumo |
Microphthalmia is a clinically and genetically heterogeneous disorder of eye development. The genetic basis of nonsyndromic microphthalmia is not yet fully understood. Previous studies indicated that disease pedigrees from different genetic backgrounds co |
| Identificador | |
| Direitos |
Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14 |
| Fonte |
Li, H; Wang, JX; Wang, CY; Yu, P; Zhou, Q; Chen, YG; Zhao, LH; Zhang, YP.Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14,122,589-593,(SCI-E ): |
| Palavras-Chave | #Genetics & Heredity |
| Tipo |
期刊论文 |
