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Annals of Human Genetics|December 27, 2024
Genotype and Haplotype Analysis With In Silico Prediction of TMPRSS2 Gene in Jordanian PopulationRazan Issam Abu-Almfalfal, Yazun Bashir Jarrar, Munir GharaibehAnnals of Human Genetics|December 24, 2024
Identifying a Genetic Link Between Lung Function and PsoriasisKazuya Tanimura, Melinda C Aldrich, James Jaworski, et al.Annals of Human Genetics|November 22, 2024
Intermittent episodes of acute severe encephalomyopathy and early death in two siblings caused by biallelic likely pathogenic variants in FASTKD2: Expanding phenotype and literature reviewNamanpreet Kaur, Puneeth H Somashekar, Sekar Deepha, et al.Annals of Human Genetics|November 12, 2024
Gastroesophageal reflux disease increases predisposition to severe COVID-19: Insights from integrated Mendelian randomization and genetic analysisJingjing Pan, Jianhua LiAnnals of Human Genetics|February 26, 2025
Exploring and Expanding Secondary Findings Through Exome Sequencing in the Turkish PopulationMehmet Berkay Akcan, Canan Ceylan Köse, Kübra Müge Çelik, et al.Annals of Human Genetics|August 29, 2024
Effects of BRCA variation on prognosis in patients with nonmetastatic breast cancerAlper Türkel, Ilknur Deliktaş Onur, Hicran Anik, et al.Annals of Human Genetics|August 2, 2024
First report of an Ivorian family with nonsyndromic hearing loss caused by GJB2 compound heterozygous variantsMadoussou Toure, Ghita Amalou, Imane Ait Raise, et al.Annals of Human Genetics|July 1, 2024
Increased prevalence of the null allele of the p.Arg577Ter variant in the ACTN3 gene in Brazilian long-distance athletes: A retrospective studyJoão Paulo Limongi França Guilherme, Edilamar Menezes OliveiraAnnals of Human Genetics|April 22, 2006
RISCALW: a Windows program for risk calculation in families with Duchenne muscular dystrophyC Fischer, J Krüger, W GrossPageof 231