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Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome.

The Wiskott-Aldrich syndrome (IMD2) is an X-linked recessive immunodeficiency. Initial linkage studies mapped the disease locus on the proximal short arm of the X chromosome, a localization which was further refined to the interval framed by DXS7 and DXS14. We have recently shown that a novel hyperv...

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Detalhes bibliográficos
Main Authors: Arveiler, B, de Saint-Basile, G, Fischer, A, Griscelli, C, Mandel, J L
Formato: Artigo
Idioma:Inglês
Publicado em: 1990
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683605/
https://ncbi.nlm.nih.gov/pubmed/1971143
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