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Annals of Human Genetics|June 15, 2018
Association of ABCG2 polymorphisms with ischemic stroke in a Chinese populationTonghanyu Liu, Feng Jiang, Xin Liu, et al.Annals of Human Genetics|July 18, 2018
CRISPR-Cas9: A cornerstone for the evolution of precision medicineSleiman RazzoukAnnals of Human Genetics|July 18, 2018
Neurofibromatosis type I: mutation spectrum of NF1 in spanish patientsCarmen Palma Milla, José Miguel Lezana Rosales, Javier López Montiel, et al.Annals of Human Genetics|October 21, 2009
Optimal robust two-stage designs for genome-wide association studiesThuy Trang Nguyen, Roman Pahl, Helmut SchäferAnnals of Human Genetics|May 20, 2017
Autosomal Recessive Nonsyndromic Arrhythmogenic Right Ventricular Cardiomyopathy without Cutaneous Involvements: A Novel MutationMahdieh Soveizi, Bahareh Rabbani, Yousef Rezaei, et al.Annals of Human Genetics|March 6, 2010
Common susceptibility variants examined for association with dilated cardiomyopathyEvadnie Rampersaud, Daniel D Kinnamon, Kara Hamilton, et al.Annals of Human Genetics|May 19, 2018
SLC40A1 and CP single nucleotide polymorphisms in porphyria cutanea tarda patients of mixed ancestryIsabella Brasil Succi, Luís Cristóvão Pôrto, Dayse Silva, et al.Annals of Human Genetics|July 1, 1988
Maternal age in trisomyN E Morton, P A Jacobs, T Hassold, et al.Annals of Human Genetics|May 1, 1985
Human myosin heavy chain genes assigned to chromosome 17 using a human cDNA clone as probeY H Edwards, M Parkar, S Povey, et al.Annals of Human Genetics|July 1, 1985
Isolation of a cDNA clone for the human muscle specific carbonic anhydrase, CAIIIJ C Lloyd, H Isenberg, D A Hopkinson, et al.Pageof 231