The gene for Nijmegen breakage syndrome (V2) is not located on chromosome 11 [2]

American Journal of Human Genetics

Volumn 58, Issue 4, 1996, Pages 885-888

  Komatsu, K ^a   Matsuura, S ^a   Tauchi, H ^a   Endo, S ^a   Kodama, S ^a   Smeets, D ^a   Weemaes, C ^a   Oshimura, M ^a  

^a HIROSHIMA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ATAXIA TELANGIECTASIA; CHROMOSOME 11Q; DEVELOPMENTAL DISORDER; GENETIC COMPLEMENTATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; HUMAN CELL; HYBRID CELL; LETTER; MICROCEPHALY; PRIORITY JOURNAL; RADIOSENSITIVITY; SKIN FIBROBLAST; SOMATIC CELL;

ATAXIA TELANGIECTASIA; CELL SURVIVAL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; GENETIC COMPLEMENTATION TEST; GENETIC HETEROGENEITY; HUMANS; HYBRID CELLS; MICROCEPHALY; RADIATION TOLERANCE; SYNDROME;

EID: 0029871180     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)