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Journal of Medical Genetics|June 7, 2005
A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 familiesN Gaukrodger, B M Mayosi, H Imrie, et al.Journal of Medical Genetics|June 7, 2005
Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and hMSH2 gene: correction for ascertainmentF Quehenberger, H F A Vasen, H C van HouwelingenJournal of Medical Genetics|May 4, 2004
Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genesJ J McCarthy, A Parker, R Salem, et al.Journal of Medical Genetics|February 1, 1992
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of bandingP A Jacobs, C Browne, N Gregson, et al.Journal of Medical Genetics|August 3, 2005
Arteriovenous malformations in Cowden syndromeM M Turnbull, V Humeniuk, B Stein, et al.Journal of Medical Genetics|August 3, 2005
Genetic linkage of a novel autosomal dominant restrictive cardiomyopathy locusJ Zhang, A Kumar, L Kaplan, et al.Journal of Medical Genetics|April 5, 2005
A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomaliesO Demirhan, S Türkmen, G C Schwabe, et al.Journal of Medical Genetics|April 5, 2005
Ancestral RET haplotype associated with Hirschsprung's disease shows linkage disequilibrium breakpoint at -1249R M Fernandez, G Boru, A Peciña, et al.Journal of Medical Genetics|September 6, 2005
Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1A Slavotinek, S S Lee, R Davis, et al.Journal of Medical Genetics|March 25, 2005
Analysis of somatic molecular changes, clinicopathological features, family history, and germline mutations in colorectal cancer families: evidence for efficient diagnosis of HNPCC and for the existence of distinct groups of non-HNPCC familiesV Johnson, L R Lipton, C Cummings, et al.Pageof 649