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Sibs lacking characteristic features of duplication of distal 17q.

Two brothers with karyotype 46,XY,-16,+der(16),t(16;17)(q24.3;q25.1)pat are presented. It is commonly thought that duplication of distal 17q results in a clinically recognisable syndrome. Although our cases had several features often seen in patients with autosomal chromosome aberrations, they did n...

詳細記述

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書誌詳細
主要な著者: Ohdo, S, Madokoro, H, Sonoda, T, Ohba, K
フォーマット: Artigo
言語:Inglês
出版事項: 1989
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015653/
https://ncbi.nlm.nih.gov/pubmed/2664178
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