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Human Heredity|February 17, 1998
Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from SlovakiaM Plásilová, E Feráková, L Kádasi, et al.Human Heredity|April 4, 1998
Screening 25 dystrophin gene exons for deletions in Arab children with Duchenne muscular dystrophyM Z Haider, L Bastaki, Y Habib, et al.Human Heredity|April 4, 1998
Fluorescence in situ hybridization of psu dic(X)(Xpter-Xq21::Xq21-Xpter) in two patients with Turner's syndromeR Fernández, E PásaroHuman Heredity|April 4, 1998
G6PD variants in three South American ethnic groups: population distribution and description of two new mutationsT A Weimer, F M Salzano, B Westwood, et al.Human Heredity|November 14, 2003
Haplotype frequency estimation in the presence of genotyping errorsGuohua Zou, Hongyu ZhaoHuman Heredity|January 1, 1992
Characterization of a 28-kD polymorphic polypeptide detected by two-dimensional electrophoresis of human plateletsS Iwamoto, E Kajii, T Omi, et al.Human Heredity|January 1, 1992
Effective population size of a rural village on a large plain (Veggiano, Padua, Italy)S Presciuttini, G U Caravello, A BaroniHuman Heredity|January 1, 1992
Deletional types of alpha-thalassaemia in central JavaJ A Tan, J S Tay, A Soemantri, et al.Human Heredity|January 1, 1992
Type II hereditary angio-oedema associated with two mutations in one allele of the C1-inhibitor gene around the reactive-site coding regionZ Siddique, A R McPhaden, K WhaleyPageof 237