TY  - GEN
AU  - Matsuura,S
AU  - Weemaes,C
AU  - Smeets,D
AU  - Takami,H
AU  - Kondo,N
AU  - Sakamoto,S
AU  - Yano,N
AU  - Nakamura,A
AU  - Tauchi,H
AU  - Endo,S
AU  - Oshimura,M
AU  - Komatsu,K
TI  - Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24
SN  - 0002-9297
PY  - 1997///0710
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Ataxia Telangiectasia
KW  - Cell Fusion
KW  - Cell Line, Transformed
KW  - Cell Survival
KW  - radiation effects
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 8
KW  - DNA Replication
KW  - Dwarfism
KW  - Genetic Complementation Test
KW  - Genetic Techniques
KW  - Humans
KW  - Immunologic Deficiency Syndromes
KW  - Microcephaly
KW  - Microsatellite Repeats
KW  - Polymerase Chain Reaction
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1086/515461
ER  -