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American Journal of Human Genetics|May 1, 1995
Mutations in the human Ca(2+)-sensing-receptor gene that cause familial hypocalciuric hypercalcemiaY H Chou, M R Pollak, M L Brandi, et al.American Journal of Human Genetics|May 1, 1995
Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11W H Raskind, E U Conrad, H Chansky, et al.American Journal of Human Genetics|May 1, 1995
Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndromeE Nickerson, F Greenberg, M T Keating, et al.American Journal of Human Genetics|April 1, 1995
Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein geneJ Liu, T M Fujiwara, N T Buu, et al.American Journal of Human Genetics|April 1, 1995
Insertion of an Alu sequence in the Ca(2+)-sensing receptor gene in familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidismN Janicic, Z Pausova, D E Cole, et al.American Journal of Human Genetics|April 1, 1995
A gene for cleidocranial dysplasia maps to the short arm of chromosome 6G J Feldman, N H Robin, L A Brueton, et al.American Journal of Human Genetics|April 1, 1995
Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31J Szabó, B Heath, V M Hill, et al.American Journal of Human Genetics|April 1, 1995
Human T-cell receptor V beta gene polymorphism and multiple sclerosisS Wei, P Charmley, R I Birchfield, et al.American Journal of Human Genetics|April 1, 1995
Demographic history of India and mtDNA-sequence diversityJ L Mountain, J M Hebert, S Bhattacharyya, et al.American Journal of Human Genetics|August 1, 1993
VNTR and microsatellite polymorphisms within the subtelomeric region of 7qA V Hing, C Helms, H Donis-KellerPageof 980