Yüklüyor......
Discontinuous microduplications at chromosome 10q24.31 identified in a Chinese family with split hand and foot malformation
BACKGROUND: Split hand/foot malformation (SHFM) is a congenital disorder characterized by a cleft of the hands and/or feet due to dificiency of central rays. Genomic rearrangement at 10q24 has been found to cause nonsyndromic SHFM (SHFM3). METHODS: Four patients and fourteen unaffected individuals f...
Kaydedildi:
| Asıl Yazarlar: | , , , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2013
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3637097/ https://ncbi.nlm.nih.gov/pubmed/23596994 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-14-45 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|