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Human Genetics|December 1, 1992
Non-radioactive detection of the most common mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex allele-specific polymerase chain reactionP Fortina, R Conant, G Monokian, et al.Human Genetics|June 18, 2003
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13Lisbeth Tranebjaerg, Tanya M Teslovich, MaryPat Jones, et al.Human Genetics|September 19, 2003
Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility lociSarah H Shaw, Jochen Hampe, Ray White, et al.Human Genetics|November 22, 2021
Genetic therapies for neurological disordersLaura FitzPatrick, Adrian BirdHuman Genetics|September 1, 1987
Genetic hemochromatosis and HLA linkageL W Powell, J Ferluga, J W Halliday, et al.Human Genetics|March 15, 2021
A missense variant in NUF2, a component of the kinetochore NDC80 complex, causes impaired chromosome segregation and aneuploidy associated with microcephaly and short statureDaniela Tiaki Uehara, Hiroshi Mitsubuchi, Johji InazawaHuman Genetics|December 3, 2021
Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferationR J Longchamps, S Y Yang, C A Castellani, et al.Human Genetics|November 25, 2021
A novel complex genomic rearrangement affecting the KCNJ2 regulatory region causes a variant of Cooks syndromeLuigia Cinque, Lucia Micale, Elena Manara, et al.Human Genetics|January 1, 1986
Sister chromatid exchange in immature haemopoietic cells, T- and B-lymphocytesP E Crossen, J M Godwin, M P BodgerHuman Genetics|February 1, 1986
Sister chromatid exchange in highly purified human B and T lymphocytesK MillerPageof 959