Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.

Nijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder characterized by microcephaly, a birdlike face, growth retardation, immunodeficiency, lack of secondary sex characteristics in females, and increased incidence of lymphoid cancers. NBS cells display a phenotype similar to that o...

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Detalhes bibliográficos
Main Authors: Cerosaletti, K M, Lange, E, Stringham, H M, Weemaes, C M, Smeets, D, Sölder, B, Belohradsky, B H, Taylor, A M, Karnes, P, Elliott, A, Komatsu, K, Gatti, R A, Boehnke, M, Concannon, P
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377248/
https://ncbi.nlm.nih.gov/pubmed/9634525
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