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Familial radioulnar synostosis.

A family with proximal radioulnar synostosis segregating in three generations is described. Familial radioulnar synostosis is a rare anomaly; however, the sporadic form is a frequent feature in cases of sex chromosome abnormalities and other syndromes. This disorder has been reported in several ethn...

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Kaydedildi:
Detaylı Bibliyografya
Yazar: Spritz, R A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1978
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1013669/
https://ncbi.nlm.nih.gov/pubmed/641954
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