Showing results (151-160 of 2,509) with videos related to

Sort By:
Pageof 251
Molecular Genetics & Genomic Medicine|February 6, 2014
The CDC Hemophilia B mutation project mutation list: a new online resourceTengguo Li, Connie H Miller, Amanda B Payne, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract developmentJ M Darlow, M G Dobson, R Darlay, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiencySali M K Farhan, Jian Wang, John F Robinson, et al.
Molecular Genetics & Genomic Medicine|January 25, 2017
hg19K: addressing a significant lacuna in hg19-based variant callingSavita Karthikeyan, Pushpinder S Bawa, Subhashini Srinivasan
Molecular Genetics & Genomic Medicine|January 25, 2017
CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosisGordon K C Leung, Dingge Ying, Christopher C Y Mak, et al.
Molecular Genetics & Genomic Medicine|January 25, 2017
Sherpas share genetic variations with Tibetans for high-altitude adaptationSushil Bhandari, Xiaoming Zhang, Chaoying Cui, et al.
Molecular Genetics & Genomic Medicine|March 23, 2019
Mild phenotype in Molybdenum cofactor deficiency: A new patient and review of the literatureBarbara Scelsa, Serena Gasperini, Andrea Righini, et al.
Molecular Genetics & Genomic Medicine|March 22, 2019
IGNITE network: Response of patients to genomic medicine interventionsLori A Orlando, Corrine Voils, Carol R Horowitz, et al.
Molecular Genetics & Genomic Medicine|April 4, 2019
Association between polymorphisms of MIR17HG and risk of colorectal cancer in the Chinese Han populationPeng Chen, Yuwei Bai, Yaru Li, et al.
Molecular Genetics & Genomic Medicine|April 6, 2019
The association of nucleotide-binding oligomerization domain 2 gene polymorphisms with the risk of asthma in the Chinese Han populationXulong Cai, Qiaolan Xu, Chenrong Zhou, et al.
Pageof 251