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Del(3) (p25.3) without phenotypic effect.

A terminal deletion of chromosome 3 at p25.3 was observed during prenatal diagnosis. A similar deletion is also present in the phenotypically normal mother. The deletion was confirmed by FISH. The breakpoint is distal to the region responsible for the 3p- syndrome. A normal baby girl was born with n...

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Detalhes bibliográficos
Main Authors: Knight, L A, Yong, M H, Tan, M, Ng, I S
Formato: Artigo
Idioma:English
Publicado em: 1995
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051787/
https://ncbi.nlm.nih.gov/pubmed/8825934
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