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Journal of Human Genetics|May 29, 2002
Microdeletions of a Y-specific marker, Yfm1, and implications for a role in spermatogenesisAshraf A Ewis, Juwon Lee, Toshikatsu Shinka, et al.Journal of Human Genetics|July 29, 2021
Genetics of autosomal mosaic chromosomal alteration (mCA)Xiaoxi Liu, Yoichiro Kamatani, Chikashi TeraoJournal of Human Genetics|October 28, 2016
Molecular analysis of 23 Pakistani families with autosomal recessive primary microcephaly using targeted next-generation sequencingRongrong Wang, Amjad Khan, Shirui Han, et al.Journal of Human Genetics|November 25, 2016
A combined linkage and association strategy identifies a variant near the GSTP1 gene associated with BMI in the Mexican populationHugo Villamil-Ramírez, Paola León-Mimila, Luis R Macias-Kauffer, et al.Journal of Human Genetics|November 25, 2016
The investigation of the origin of Southern Tunisians using HLA genesAbdelhafidh Hajjej, Wassim Y Almawi, Lasmar Hattab, et al.Journal of Human Genetics|November 25, 2016
Comparison of exome-based HLA class I genotyping tools: identification of platform-specific genotyping errorsKazuma Kiyotani, Tu H Mai, Yusuke NakamuraJournal of Human Genetics|January 31, 2008
R1467H variant in the rho guanine nucleotide exchange factor 11 (ARHGEF11) is associated with impaired glucose tolerance and type 2 diabetes in German CaucasiansYvonne Böttcher, Dorit Schleinitz, Anke Tönjes, et al.Journal of Human Genetics|December 18, 2007
Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani familiesMuhammad S Chishti, Attya Bhatti, Sana Tamim, et al.Journal of Human Genetics|February 20, 2008
Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangismWei Yang, Lihua Cao, Wenli Liu, et al.Journal of Human Genetics|March 21, 2014
Signature of backward replication slippage at the copy number variation junctionTamae Ohye, Hidehito Inagaki, Mamoru Ozaki, et al.Pageof 352