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

American Journal of Human Genetics

Volumn 60, Issue 6, 1997, Pages 1487-1494

  Matsuura, Shinya ^a   Weemaes, Corry ^b   Smeets, Dominique ^b   Takami, Hideki ^a   Kondo, Noriko ^a   Sakamoto, Shuuichi ^a   Yano, Nozomi ^a   Nakamura, Asako ^a   Tauchi, Hiroshi ^a   Endo, Satoru ^a   Oshimura, Mitsuo ^c   Komatsu, Kenshi ^a  

^a HIROSHIMA UNIVERSITY   (Japan)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c TOTTORI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ATAXIA TELANGIECTASIA; CHROMOSOME 8Q; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; GENE LOCUS; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC STABILITY; HUMAN; HUMAN CELL; HUMAN TISSUE; IONIZING RADIATION; NIJMEGEN BREAKAGE SYNDROME; PRIORITY JOURNAL; SYNDROME DELINEATION;

ATAXIA; ATAXIA TELANGIECTASIA;

EID: 16944367119     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/515461     Document Type: Article

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