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Human Heredity|June 9, 1998
Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21M A Nance, W A Raabe, H Midani, et al.Human Heredity|January 1, 1989
HLA antigens in three populations of IndiaS S Papiha, J Wentzel, K C Shah, et al.Human Heredity|January 1, 1989
Frequency of the ESD*5 allele in a Spanish populationP Moreno, J Más, G RibóHuman Heredity|February 17, 1998
Detection of genetic structures at short distances in the Pisa areaE Mamolini, M Beretta, R Barale, et al.Human Heredity|February 17, 1998
Identification of two novel mutations in the hydroxymethylbilane synthase gene in three patients from two unrelated families with acute intermittent porphyriaP M Ong, W G Lanyon, R J Hift, et al.Human Heredity|February 17, 1998
Factor VIII gene inversions in haemophilia A patients of SlovakiaH Poláková, L Kádasi, A FilováHuman Heredity|February 17, 1998
Association between variants of mast cell chymase gene and serum IgE levels in eczemaX Q Mao, T Shirakawa, T Enomoto, et al.Human Heredity|February 17, 1998
Estimating recombination fraction separately for males and females: a counterintuitive resultS E Hodge, P L Flodman, M F Duryea, et al.Human Heredity|January 1, 1976
The association of blood groups, ABH secretion, haptoglobins and hemoglobins with filariasisM Ayres, F M Salzano, M Helena, et al.Pageof 237