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Human Genetics|October 1, 1987
Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11J S Waye, G M Greig, H F WillardHuman Genetics|October 1, 1987
Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)S Malcolm, G de Saint Basile, B Arveiler, et al.Human Genetics|April 1, 1988
DNA polymorphism and the study of disease associationsD N Cooper, J F ClaytonHuman Genetics|April 1, 1988
Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic RepublicO Riess, A Michel, A Speer, et al.Human Genetics|July 18, 1979
Biochemical genetic markers in the Kadazans of Sabah, MalaysiaS G Tan, Y S Teng, J Ganesan, et al.Human Genetics|May 1, 1988
Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresisJ Morreau, M Sinaasappel, B A Oostra, et al.Human Genetics|December 1, 1987
Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1----q22.3 in a patient with tyrosinemia type IIE Natt, E M Westphal, S E Toth-Fejel, et al.Human Genetics|December 1, 1987
The study of a French family with two duplicated C4A haplotypesC M Giles, B Uring-Lambert, W Boksch, et al.Human Genetics|December 1, 1987
Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasiaF Marlhens, J Chelly, J C Kaplan, et al.Human Genetics|September 4, 2017
Recent advances in assays for the fragile X-related disordersBruce E Hayward, Daman Kumari, Karen UsdinPageof 958