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Human Genetics|July 1, 1997
Regional distribution of beta-thalassemia mutations in IndiaI C Verma, R Saxena, E Thomas, et al.Human Genetics|November 8, 2005
Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33-q27.3Peter John, Ghazanfar Ali, Muhammad S Chishti, et al.Human Genetics|September 1, 1992
Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNAC S Mgone, W G Lanyon, M R Moore, et al.Human Genetics|September 1, 1992
Molecular genotyping of N-acetylation polymorphism to predict phenotypeM Mashimo, T Suzuki, M Abe, et al.Human Genetics|September 1, 1992
Multiple minute marker chromosomes derived from Y identified by FISH in an intersexual infantL Diekmann, K Palm, R A Pfeiffer, et al.Human Genetics|September 1, 1992
Prenatal diagnosis of Duchenne muscular dystrophy by fetal muscle biopsyJ A Kuller, E P Hoffman, M H Fries, et al.Human Genetics|September 1, 1992
Significance of the clonal and sporadic chromosome abnormalities in non-neoplastic renal tissueR Casalone, P Granata Casalone, E Minelli, et al.Human Genetics|September 1, 1992
A genetic study of the human low-voltage electroencephalogramA Anokhin, O Steinlein, C Fischer, et al.Human Genetics|May 1, 1986
The pro alpha 2(V) collagen gene (COL5A2) maps to 2q14----2q32, syntenic to the pro alpha 1 (III) collagen locus (COL3A1)C Huerre-Jeanpierre, I Henry, M Bernard, et al.Pageof 958