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Underlying genetic factors of the VATER/VACTERL association with special emphasis on the “Renal” phenotype
The acronym VATER/VACTERL association (OMIM #192350) refers to the rare non-random co-occurrence of the following component features (CFs): vertebral defects (V), anorectal malformations (A), cardiac defects (C), tracheoesophageal fistula with or without esophageal atresia (TE), renal malformations...
Kaydedildi:
| Yayımlandı: | Pediatr Nephrol |
|---|---|
| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5207487/ https://ncbi.nlm.nih.gov/pubmed/26857713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-016-3335-3 |
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