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Human Molecular Genetics|January 1, 1996
Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175K A Brown, A H Janjua, G Karbani, et al.
American Journal of Human Genetics|December 1, 1999
The genetic epidemiology of early-onset epithelial ovarian cancer: a population-based studyJ F Stratton, D Thompson, L Bobrow, et al.
American Journal of Human Genetics|August 10, 2000
Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndromeC A Hobbs, S L Sherman, P Yi, et al.
British Journal of Cancer|July 2, 1999
Mutation testing in melanoma families: INK4A, CDK4 and INK4DJ A Newton Bishop, M Harland, D C Bennett, et al.
Epidemiology (Cambridge, Mass.)|October 14, 2005
HFE genotype modifies the influence of heme iron intake on iron statusD C Greenwood, J E Cade, J A Moreton, et al.
Human Molecular Genetics|January 4, 2001
A germline deletion of p14(ARF) but not CDKN2A in a melanoma-neural system tumour syndrome familyJ A Randerson-Moor, M Harland, S Williams, et al.
American Journal of Human Genetics|September 1, 1991
Trisomy 21: association between reduced recombination and nondisjunctionS L Sherman, N Takaesu, S B Freeman, et al.
Human Reproduction (Oxford, England)|June 26, 2007
Examination of reproductive aging milestones among women who carry the FMR1 premutationE G Allen, A K Sullivan, M Marcus, et al.
American Journal of Human Genetics|March 1, 1996
Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based studyP W Yoon, S B Freeman, S L Sherman, et al.
Oncology Reports|August 13, 2013
Plasma osteopontin concentrations in patients with cutaneous melanomaA Filia, F Elliott, T Wind, et al.
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