Showing results (21-30 of 222) with videos related to
Sort By:
Pageof 23
American Journal of Medical Genetics|December 1, 1988
Recurrence risks for relatives in families with an isolated case of the fragile X syndromeS L Sherman, A Rogatko, G TurnerClinical and Experimental Dermatology|January 23, 1999
The genetics of melanoma: the UK experienceJ A Newton Bishop, M Harland, D T BishopBMC Genetics|February 21, 2004
Segregation analysis comparing liability and quantitative trait models for hypertension using the Genetic Analysis Workshop 13 simulated dataG P Crockford, D T Bishop, J H BarrettGut|November 21, 1998
Are relatives of patients with multiple HNPCC spectrum tumours at increased risk of cancer?S R Brown, P J Finan, D T BishopAmerican Journal of Human Genetics|September 1, 1983
A model for restriction fragment length distributionsD T Bishop, J A Williamson, M H SkolnickAmerican Journal of Human Genetics|January 1, 1996
Statistical models for trisomic phenotypesN E Lamb, E Feingold, S L ShermanAmerican Journal of Human Genetics|March 11, 2000
Multipoint estimation of genetic maps for human trisomies with one parent or other partial dataE Feingold, A S Brown, S L ShermanHuman Molecular Genetics|November 25, 2000
Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCRD C Crawford, B Wilson, S L ShermanAmerican Journal of Human Genetics|February 1, 1995
Methods for genetic linkage analysis using trisomiesE Feingold, N E Lamb, S L ShermanGenomics|June 1, 1993
Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage mapS Todd, S L Sherman, S L NaylorPageof 23