Occurrence of Synpolydactyly and Omphalocele in a Fetus with a HOXD13 Mutation

Synpolydactyly (SPD) is an autosomal dominant congenital limb disorder due to mutations in HOXD13 . It is a phenotypically heterogeneous condition characterized by syndactyly of the third finger (F3), fourth finger (F4) and/or fourth toe (T4), and fifth toe (T5) with variably associated polydactyly....

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Detaylı Bibliyografya
Yayımlandı:J Pediatr Genet
Asıl Yazarlar: Radhakrishnan, Periyasamy, Nayak, Shalini S., Pai, Muralidhar V., Shukla, Anju, Girisha, Katta M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Georg Thieme Verlag KG 2017
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5548533/
https://ncbi.nlm.nih.gov/pubmed/28794915
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0037-1602142
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