Showing results (41-50 of 2,300) with videos related to

Sort By:
Pageof 230
Annals of Human Genetics|March 20, 2019
Influence of STAT4 gene polymorphisms in the pathogenesis of endometriosisBianca Bianco, Ramon Felix Martins Fernandes, Camila Martins Trevisan, et al.
Annals of Human Genetics|March 20, 2019
Association of single nucleotide polymorphisms in TPM1 rs11071720, rs3803499, rs12148828, and rs1972041 with the risk of nonsyndromic cleft lip with or without cleft palate in a sample of the Iranian population, a preliminary reportHoushang Rafighdoost, Fatemeh Tabatabaei, Gholamreza Bahari, et al.
Annals of Human Genetics|March 20, 2019
Two novel variants in the ATM gene causing ataxia-telangiectasia, including a duplication of 90 kb: Utility of targeted next-generation sequencing in detection of copy number variationSamuel Martin-Rodriguez, Alicia Calvo-Ferrer, Nerea Ortega-Unanue, et al.
Annals of Human Genetics|August 17, 2019
Argentinian clinical genomics in a leukodystrophies and genetic leukoencephalopathies cohort: Diagnostic yield in our first 9 yearsLeila Cohen, Analisa Manín, Nancy Medina, et al.
Annals of Human Genetics|July 30, 2019
Congenital microcephaly-linked CDK5RAP2 affects eye developmentSami Zaqout, Ethiraj Ravindran, Gisela Stoltenburg-Didinger, et al.
Annals of Human Genetics|December 13, 2021
Frequency of DPYD gene variants and phenotype inference in a Southern Brazilian populationMariana Rodrigues Botton, Marina Hentschke-Lopes, Ursula Matte
Annals of Human Genetics|March 22, 2019
Association of rs10490924 in ARMS2/HTRA1 with age-related macular degeneration in the Pakistani populationHumaira Ayub, Sobia Shafique, Aisha Azam, et al.
Annals of Human Genetics|March 22, 2019
Population genetics of 15 autosomal STR loci in the Han population of Ili Kazakh Autonomous Prefecture, Northwestern ChinaZhi-Liang Zhao, Lu Xia, Cong Zhao, et al.
Annals of Human Genetics|December 28, 2021
The molecular landscape of progressive familial intrahepatic cholestasis in Turkey: Defining the molecular profiles and expanding the variant spectrumAbdullatif Bakır, Vehap Topçu, Büşranur Çavdarlı
Annals of Human Genetics|February 22, 2012
Relevance of SOX17 variants for hypomyelinating leukodystrophies and congenital anomalies of the kidney and urinary tract (CAKUT)Patricia Combes, Vincent Planche, Eléonore Eymard-Pierre, et al.
Pageof 230