Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24.

Nijmegen breakage syndrome (NBS) is an autosomal recessive disorder characterized by microcephaly, short stature, immunodeficiency, and a high incidence of cancer. Cultured cells from NBS show chromosome instability, an increased sensitivity to radiation-induced cell killing, and an abnormal cell-cy...

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Main Authors: Matsuura, S, Weemaes, C, Smeets, D, Takami, H, Kondo, N, Sakamoto, S, Yano, N, Nakamura, A, Tauchi, H, Endo, S, Oshimura, M, Komatsu, K
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1716114/
https://ncbi.nlm.nih.gov/pubmed/9199571
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