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Molecular and cytogenetic analysis of a familial microdeletion of Xq.

Cytogenetic analysis of a male infant referred for poor neurological development and failure to thrive showed a microdeletion of the X chromosome, his karyotype being 46,Y,del(X)(pter----q21.1:: q21.2----qter). His mother and grandmother were also found to carry the deletion. DNA probes were used to...

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Main Authors: Wells, S, Mould, S, Robins, D, Robinson, D, Jacobs, P
格式: Artigo
語言:Inglês
出版: 1991
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016798/
https://ncbi.nlm.nih.gov/pubmed/1675684
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