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Elucidation of the centromere involvement in an inversion (13) by fluorescent in situ hybridisation.

A newborn infant with phenotypic features of trisomy for distal 13q was found to have recombinant inversion duplication involving the (13)(q22-->qter) region. Parental karyotypes showed that the mother had a normal 46,XX complement and the father had an apparently balanced pericentric inversion o...

詳細記述

保存先:
書誌詳細
主要な著者: Gordon, P L, Dalton, J D, Martens, P R, Tharapel, A T, Wilroy, R S
フォーマット: Artigo
言語:Inglês
出版事項: 1993
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016380/
https://ncbi.nlm.nih.gov/pubmed/8320705
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