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Human Genetics|August 7, 2024
GBF1 deficiency causes cataracts in human and mouseWeimin Jia, Chenming Zhang, Yalin Luo, et al.Human Genetics|September 1, 1991
The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2-p36.3O Kemper, J Derré, D Cherif, et al.Human Genetics|March 31, 2006
Common chromatin structures at breakpoint cluster regions may lead to chromosomal translocations found in chronic and acute leukemiasReiner Strick, Yanming Zhang, Neelmini Emmanuel, et al.Human Genetics|March 30, 2006
Genome-wide linkage analysis of population variation in high-density lipoprotein cholesterolStephen B Harrap, Zilla Y H Wong, Katrina J Scurrah, et al.Human Genetics|August 1, 1991
Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyriaJ S Lee, G Lundin, L Lannfelt, et al.Human Genetics|March 22, 2006
Allelic spectrum of the natural variation in CRPDana C Crawford, Qian Yi, Joshua D Smith, et al.Human Genetics|March 23, 2006
Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic miceLaurent Foiry, Li Dong, Cédric Savouret, et al.Human Genetics|July 1, 1991
Human polymorphic probe pE1.8 detects SacI polymorphism in the ribonucleotide reductase M1 subunit geneJ Byrne, P SmithHuman Genetics|June 20, 2006
The microcell-mediated transfer of human chromosome 8 restores the deficient N-acetylytransferase activity in skin fibroblasts of Mucopolysaccharidosis type IIIC patientsVolkan Seyrantepe, Frédérique Tihy, Alexey V PshezhetskyHuman Genetics|June 20, 2006
Variants in the HEPSIN gene are associated with prostate cancer in men of European originProdipto Pal, Huifeng Xi, Ritesh Kaushal, et al.Pageof 957