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American Journal of Human Genetics|October 6, 2000
Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndromeY Q Wu, J L Badano, C McCaskill, et al.
American Journal of Human Genetics|October 18, 2000
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetesS Ghosh, R M Watanabe, T T Valle, et al.
American Journal of Human Genetics|October 18, 2000
Performance of Markov chain-Monte Carlo approaches for mapping genes in oligogenic models with an unknown number of lociJ K Lee, D C Thomas
American Journal of Human Genetics|October 18, 2000
Tracing European founder lineages in the Near Eastern mtDNA poolM Richards, V Macaulay, E Hickey, et al.
American Journal of Human Genetics|September 28, 2000
Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helixA J Richards, D M Baguley, J R Yates, et al.
American Journal of Human Genetics|September 28, 2000
Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brainT de los Santos, J Schweizer, C A Rees, et al.
American Journal of Human Genetics|August 26, 2000
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group GA C Muntau, P U Mayerhofer, B C Paton, et al.
American Journal of Human Genetics|August 26, 2000
Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophyA Maugeri, B J Klevering, K Rohrschneider, et al.
American Journal of Human Genetics|August 30, 2000
A unified Haseman-Elston method for testing linkage with quantitative traitsX Xu, S Weiss, X Xu, et al.
American Journal of Human Genetics|September 14, 2000
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type BG C Schwabe, S Tinschert, C Buschow, et al.
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