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Human Genetics|December 14, 2006
A case of true hermaphroditism reveals an unusual mechanism of twinningVivienne L Souter, Melissa A Parisi, Dale R Nyholt, et al.Human Genetics|October 1, 1991
Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndromeG Van Camp, H Backhovens, M Cruts, et al.Human Genetics|October 1, 1991
A frameshift mutation in exon 2 of the phenylalanine hydroxylase gene linked to RFLP haplotype 1A Eigel, B Dworniczak, L Kalaydjieva, et al.Human Genetics|October 1, 1991
Detection of frequent BglII polymorphism by polymerase chain reaction and TaqI restriction fragment length polymorphism for 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4 isomerase at the human HSD beta 3 locus (1p11-p13)E Rhéaume, J F Leblanc, Y Lachance, et al.Human Genetics|November 1, 1991
Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndromeC A Gregory, J Schwartz, A J Kirkilionis, et al.Human Genetics|May 20, 2006
No association between complement factor H gene polymorphism and exudative age-related macular degeneration in JapaneseNorimoto Gotoh, Ryo Yamada, Hitomi Hiratani, et al.Human Genetics|August 1, 1986
The rate of chromosome breakage is age dependent in lymphocytes of adult controlsF Marlhens, W A Achkar, A Aurias, et al.Human Genetics|August 1, 1986
The polymorphism of desialyzed alpha 2HS-glycoprotein (AHS): isoelectric focusing in 2.5 M urea as a method for identification of genetic variantsK Umetsu, I Yuasa, T SuzukiHuman Genetics|August 1, 1986
Inverted neurons in agyria. A Golgi study of a case with abnormal chromosome 17C Bordarier, O Robain, M O Rethoré, et al.Pageof 957