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Prenatal Diagnosis|February 1, 1995
An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell lineD A Batista, C Escallon, K J Blakemore, et al.Human Molecular Genetics|August 1, 2000
A cre-lox recombination system for the targeted integration of circular yeast artificial chromosomes into embryonic stem cellsL M Call, C S Moore, G Stetten, et al.Experimental Hematology|September 1, 1988
The human Jurkat (FHCRC-11) cell line is heterogeneous in ploidy and cell size and releases detergent-soluble DNAK A LaGree, A T Lee, G Stetten, et al.American Journal of Human Genetics|August 1, 1986
Translocation of the nucleolus organizer region to the human X chromosomeG Stetten, B Sroka, M Schmidt, et al.Genomics|January 8, 1999
Genomic structure of PEX13, a candidate peroxisome biogenesis disorder geneJ Björkman, G Stetten, C S Moore, et al.In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|October 1, 1991
Origin of chromosome rearrangements in two long-lived human keratinocyte linesC Rosenberg, G Stetten, W G Kearns, et al.Proceedings of the National Academy of Sciences of the United States of America|October 10, 1995
TRPC1, a human homolog of a Drosophila store-operated channelP D Wes, J Chevesich, A Jeromin, et al.Obstetrics and Gynecology|September 1, 1992
Fetal ascitic fluid: a new source of lymphocytes for rapid chromosomal analysisJ R Wax, K J Blakemore, M J Soloski, et al.Journal of the National Cancer Institute|May 6, 1992
Promoting smoking cessation in the United States: effect of public service announcements on the Cancer Information Service telephone lineJ P Pierce, D M Anderson, R M Romano, et al.Somatic Cell and Molecular Genetics|March 1, 1995
Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivationB R Migeon, G Stetten, C Tuck-Muller, et al.Pageof 7