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Annals of Human Genetics|October 1, 1989
Subtypes of HLA-DQ and -DR defined by DQB1 and DRB1 RFLPs: allele frequencies in the general population and in insulin-dependent diabetes (IDDM) and multiple sclerosis patientsK J Gogolin, V J Kolaga, L Baker, et al.Annals of Human Genetics|March 18, 2015
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1Francesco Nicita, Fiorenza Ulgiati, Laura Bernardini, et al.Annals of Human Genetics|August 8, 2020
Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencingDarine Villela, Juliana Sobral de Barros, Silvia Souza da Costa, et al.Annals of Human Genetics|September 14, 2012
Robustness of Bayesian multilocus association models to cryptic relatednessHanni P Kärkkāinen, Mikko J SillanpääAnnals of Human Genetics|September 5, 2012
Identification and confirmation of an exonic splicing enhancer variation in exon 5 of the Alzheimer disease associated PICALM geneNathalie C Schnetz-Boutaud, Joshua Hoffman, Jared E Coe, et al.Annals of Human Genetics|October 1, 1988
Cloning and chromosomal mapping of human cytochrome b5 reductase (DIA1)P C Bull, E A Shephard, S Povey, et al.Annals of Human Genetics|June 26, 2012
Transforming growth factor β1-509C/T and +869T/C polymorphisms on the risk of upper digestive tract cancer: a meta-analysis based on 10,917 participantsCai-Feng Zhang, Zhong-Wei Wang, Meng-Xia Hou, et al.Annals of Human Genetics|January 1, 1979
A comparison of the biochemical properties of the human diaphorase (DIA3) isozymes determined by the common alleles DIA13, DIA23 and DIA33Y H Edwards, J E Potter, D A HopkinsonAnnals of Human Genetics|January 1, 1979
Human Y chromosome variation in normal and abnormal babies and their fathersI C Beltran, F W Robertson, B M PageAnnals of Human Genetics|January 1, 1979
The genetics of palmar creases. A study in the inheritance of liability estimated from the incidence among relativesJ S TayPageof 231