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Human Heredity|January 1, 1992
A polymorphic complex dinucleotide repeat at the telomeric D8S7 locusS Wood, M Schertzer
Genome|February 1, 1997
A 2.8 megabase YAC contig spanning D8S339, which is tightly linked to the Werner syndrome locusR Bruskiewich, M Schertzer, S Wood
Somatic Cell and Molecular Genetics|March 1, 1995
Identification of the human neuronal nicotinic cholinergic alpha 2 receptor locus, (CHRNA2), within an 8p21 mapped locus, by sequence homology with rat DNAS Wood, M Schertzer, M L Yaremko
Cytogenetics and Cell Genetics|January 1, 1995
Sequence identity locates CEBPD and FGFR1 to mapped human loci within proximal 8pS Wood, M Schertzer, M L Yaremko
Human Genetics|May 1, 1993
Support for founder effect for two lipoprotein lipase (LPL) gene mutations in French Canadians by analysis of GT microsatellites flanking the LPL geneS Wood, M Schertzer, M Hayden, et al.
Clinical Genetics|August 1, 1987
Inverted tandem duplication generates a duplication deficiency of chromosome 8pF J Dill, M Schertzer, J Sandercock, et al.
Genomics|December 10, 1999
Genomic organization, expression, and chromosome location of the human SNAIL gene (SNAI1) and a related processed pseudogene (SNAI1P)W A Paznekas, K Okajima, M Schertzer, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Characterization of a human chromosome 8 cosmid library constructed from flow-sorted chromosomesS Wood, M Schertzer, H Drabkin, et al.
Genomics|August 29, 1998
Human SLUG gene organization, expression, and chromosome map location on 8qM E Cohen, M Yin, W A Paznekas, et al.
Genomics|December 1, 1994
Mapping of the pulmonary surfactant SP5 (SFTP2) locus to 8p21 and characterization of a microsatellite repeat marker that shows frequent loss of heterozygosity in human carcinomasS Wood, M L Yaremko, M Schertzer, et al.
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