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American Journal of Human Genetics|December 5, 1998
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group DM Honsho, S Tamura, N Shimozawa, et al.American Journal of Human Genetics|December 5, 1998
Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutationsS Jacquot, K Merienne, D De Cesare, et al.American Journal of Human Genetics|December 5, 1998
The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestryN A Ellis, S Ciocci, M Proytcheva, et al.American Journal of Human Genetics|December 5, 1998
Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy numberD W Parsons, P E McAndrew, S T Iannaccone, et al.American Journal of Human Genetics|December 5, 1998
The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene clusterM Vollmer, M Jung, F Rüschendorf, et al.American Journal of Human Genetics|December 5, 1998
Search for a founder mutation in idiopathic focal dystonia from Northern GermanyC Klein, L J Ozelius, J Hagenah, et al.American Journal of Human Genetics|December 5, 1998
European Y-chromosomal lineages in Polynesians: a contrast to the population structure revealed by mtDNAM E Hurles, C Irven, J Nicholson, et al.American Journal of Human Genetics|December 5, 1998
Genome screens using linkage disequilibrium tests: optimal marker characteristics and feasibilityN H Chapman, E M WijsmanAmerican Journal of Human Genetics|September 1, 1976
Specific chromosome aberrations in senescent fibroblast cell lines derived from human embryosP A BennAmerican Journal of Human Genetics|January 23, 1999
LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosisY Segal, B Peissel, A Renieri, et al.Pageof 979