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A new case of proximal 10q partial trisomy.

We report on a girl with mild phenotypic abnormalities and duplication of chromosome 10q11----10q22. The similarities to two previously reported cases with an identical chromosomal aberration provide further support for the delineation of this entity as a specific, clinically recognisable syndrome.

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Bibliografski detalji
Glavni autori: de Michelena, M I, Campos, P J
Format: Artigo
Jezik:Inglês
Izdano: 1991
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016807/
https://ncbi.nlm.nih.gov/pubmed/2051458
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