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Human Genetics|September 1, 1988
Recurrent genomic rearrangements are not at the fragile sites on chromosomes 3 and 5 in human renal cell carcinomasG Kovacs, P BrusaHuman Genetics|June 29, 2021
IFIH1 loss-of-function variants contribute to very early-onset inflammatory bowel diseaseMara Cananzi, Elizabeth Wohler, Antonio Marzollo, et al.Human Genetics|January 23, 2018
Reconstructing the demographic history of the Himalayan and adjoining populationsRakesh Tamang, Gyaneshwer Chaubey, Amrita Nandan, et al.Human Genetics|January 25, 2018
Complex signatures of natural selection at GYPAAbigail W Bigham, Kevin Magnaye, Diane M Dunn, et al.Human Genetics|August 1, 1987
Unsuitability of the assay for cell-mediated lympholysis in inbred mice for H-Y antigen determination of human cellsA Braun, H CleveHuman Genetics|November 1, 1988
Chromosome localization of the human insulin gene in transgenic mouse linesK Michalova, D Bucchini, M A Ripoche, et al.Human Genetics|July 1, 1987
Contribution of magnetic resonance imaging to the knowledge of CNS malformations related to chromosomal aberrationsJ C Tamraz, M O Rethoré, M T Iba-Zizen, et al.Human Genetics|June 9, 2022
GATA4 and estrogen receptor alpha bind at SNPs rs9921222 and rs10794639 to regulate AXIN1 expression in osteoblastsSarocha Suthon, Rachel S Perkins, Jianjian Lin, et al.Human Genetics|June 28, 2022
Clinical characteristics and comorbidities of COVID-19 in unvaccinated patients with Down syndrome: first year report in BrazilMatheus Negri Boschiero, Camila Vantini Capasso Palamim, Manoela Marques Ortega, et al.Human Genetics|April 1, 1987
Human elongation factor 1 alpha: a polymorphic and conserved multigene family with multiple chromosomal localizationsG Opdenakker, Y Cabeza-Arvelaiz, P Fiten, et al.Pageof 957