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Human Genetics|August 2, 2001
Duplication and transposition of the NF1 pseudogene regions on chromosomes 2, 14, and 22M Luijten, S Redeker, S Minoshima, et al.
Cytogenetics and Cell Genetics|January 1, 1991
The Chinese hamster cell mutant V-H4 is homologous to Fanconi anemia (complementation group A)F Arwert, M A Rooimans, A Westerveld, et al.
Biophysical Journal|June 1, 1974
Photoreactivation and excision repair of ultraviolet radiation-injured DNA in primary embryonic chick cellsM C Paterson, P H Lohman, E A de Weerd-Kastelein, et al.
Genes, Chromosomes & Cancer|February 1, 1994
Amplification of the anonymous marker D17S67 in malignant astrocytomasE K Bijlsma, S Leenstra, A Westerveld, et al.
Human Genetics|December 23, 1977
Characterization of residual hexosaminidase activity in Sandhoff's disease using man-Chinese hamster cell hybridsH L Hoeksema, A J Reuser, A T Hoogeveen, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1976
Assignment of the AK1:Np:ABO linkage group to human chromosome 9A Westerveld, A P Jongsma, P Meera Khan, et al.
Genes, Chromosomes & Cancer|October 1, 1992
Molecular characterization of chromosome 22 deletions in schwannomasE K Bijlsma, R Brouwer-Mladin, D A Bosch, et al.
Somatic Cell Genetics|July 1, 1977
Regional localization of a beta-galactosidase locus on human chromosome 22J De Wit, H L Hoeksema, D Halley, et al.
American Journal of Human Genetics|January 1, 1977
Characterization of beta-D-N-acetylhexosaminidase isoenzymes in man-Chinese hamster somatic cell hybridsH L Hoeksema, A J Reuser, A Hoogeveen, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3E Redeker, M Alders, J M Hoovers, et al.
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