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American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndromeC E Yu, J Oshima, K A Goddard, et al.American Journal of Human Genetics|August 1, 1994
A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31.3-32J Dixon, A J Gladwin, S K Loftus, et al.American Journal of Human Genetics|July 1, 1994
Molecular characterization of the marker chromosome associated with cat eye syndromeA J Mears, A M Duncan, M L Budarf, et al.American Journal of Human Genetics|July 1, 1994
Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformationS E Palmer, S W Scherer, M Kukolich, et al.American Journal of Human Genetics|July 1, 1994
Bloom syndrome and maternal uniparental disomy for chromosome 15T Woodage, M Prasad, J W Dixon, et al.American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium patterns vary with chromosomal location: a case study from the von Willebrand factor regionW S Watkins, R Zenger, E O'Brien, et al.American Journal of Human Genetics|September 1, 1994
Differential allelic expression of a fibrillin gene (FBN1) in patients with Marfan syndromeD Hewett, J Lynch, A Child, et al.American Journal of Human Genetics|October 1, 1994
Osteogenesis imperfecta type I: molecular heterogeneity for COL1A1 null alleles of type I collagenM C Willing, S P Deschenes, D A Scott, et al.American Journal of Human Genetics|October 1, 1994
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen geneM D Briggs, H Choi, M L Warman, et al.American Journal of Human Genetics|October 1, 1994
A gene for episodic ataxia/myokymia maps to chromosome 12p13M Litt, P Kramer, D Browne, et al.Pageof 980