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American Journal of Medical Genetics|May 1, 1988
Investigation of the twinning rate in families with the fragile X syndromeS L Sherman, G Turner, L Sheffield, et al.
Annals of Human Genetics|January 1, 1984
The marker (X) syndrome: a cytogenetic and genetic analysisS L Sherman, N E Morton, P A Jacobs, et al.
The British Journal of Surgery|October 1, 1994
Genetic susceptibility to colorectal cancer in patients under 45 years of ageN R Hall, P J Finan, B Ward, et al.
Gut|November 21, 1998
Frequency of replication errors in colorectal cancer and their association with family historyS R Brown, P J Finan, L Cawkwell, et al.
Cytogenetic and Genome Research|September 30, 2005
Risk factors for nondisjunction of trisomy 21S L Sherman, S B Freeman, E G Allen, et al.
Genetic Epidemiology|January 1, 1984
Genetic Analysis Workshop II: combined segregation, linkage, and association analysisN E Morton, S L Sherman, S MacLean, et al.
Genetic Epidemiology|January 1, 1988
Segregation and linkage analysis of nine Utah breast cancer pedigreesD T Bishop, L Cannon-Albright, T McLellan, et al.
Genetic Testing|May 4, 2000
Exon deletions and duplications in BRCA1 detected by semiquantitative PCRM D Robinson, C E Chu, G Turner, et al.
British Journal of Cancer|June 12, 2003
Linkage and association analysis of nevus density and the region containing the melanoma gene CDKN2A in UK twinsJ H Barrett, R Gaut, R Wachsmuth, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|March 27, 1998
Association study of asthma and atopy traits and chromosome 5q cytokine cluster markersA H Mansur, D T Bishop, A F Markham, et al.
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