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Human Genetics|December 1, 1989
Isochromosome not translocation in trisomy 21q21qM Grasso, M L Giovannucci Uzielli, M Pierluigi, et al.Human Genetics|August 27, 2014
Bayesian variable selection for hierarchical gene-environment and gene-gene interactionsChanglu Liu, Jianzhong Ma, Christopher I AmosHuman Genetics|November 30, 2014
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genesMarc Woodbury-Smith, Andrew D Paterson, Bhooma Thiruvahindrapduram, et al.Human Genetics|July 1, 1989
Detection of beta-thalassemia and hemoglobin E genes in Thai by a DNA amplification techniqueP Winichagoon, J Kownkon, P Yenchitsomanus, et al.Human Genetics|May 1, 1986
Maternal serum alpha-fetoprotein screening for neural tube defects and other disorders using an ultramicro-ELISA. Collaborative study in Cuba and in the German Democratic RepublicH Körner, L Rodriguez, J L Fernandez Yero, et al.Human Genetics|November 16, 2013
Comparative‑high resolution melting: a novel method of simultaneous screening for small mutations and copy number variationsPawel Borun, Lukasz Kubaszewski, Tomasz Banasiewicz, et al.Human Genetics|November 19, 2013
Natural and orthogonal model for estimating gene-gene interactions applied to cutaneous melanomaFeifei Xiao, Jianzhong Ma, Guoshuai Cai, et al.Human Genetics|November 19, 2013
MicroRNA-related sequence variations in human cancersA Wojcicka, A de la Chapelle, K JazdzewskiHuman Genetics|January 1, 1985
Down syndrome: increased frequency of maternal meiosis I nondisjunction during the transitional stages of the ovulatory seasonsP H Jongbloet, O J VriezeHuman Genetics|January 12, 2018
De novo variants in SETD1B are associated with intellectual disability, epilepsy and autismTakuya Hiraide, Mitsuko Nakashima, Kaori Yamoto, et al.Pageof 958