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Maternal uniparental disomy of chromosome 13 in a phenotypically normal child.

A case of maternal uniparental disomy of chromosome 13 is described. The subject is a phenotypically normal male who inherited a t(13;13)(p11.2;p11.2) from his mother who is a carrier of this translocation. The mother was ascertained through a history of recurrent abortion and is phenotypically norm...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Slater, H, Shaw, J H, Dawson, G, Bankier, A, Forrest, S M
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: 1994
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050029/
https://ncbi.nlm.nih.gov/pubmed/7815424
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