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American Journal of Human Genetics|March 20, 2001
Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cystsP A Leegwater, B Q Yuan, J van der Steen, et al.American Journal of Human Genetics|March 20, 2001
Multipoint linkage-disequilibrium-mapping approach based on the case-parent trio designK Y Liang, F C Hsu, T H Beaty, et al.American Journal of Human Genetics|March 20, 2001
Assessment of parent-of-origin effects in linkage analysis of quantitative traitsR L Hanson, S Kobes, R S Lindsay, et al.American Journal of Human Genetics|October 18, 2000
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait lociR M Watanabe, S Ghosh, C D Langefeld, et al.American Journal of Human Genetics|October 18, 2000
Improved inference of relationship for pairs of individualsM P Epstein, W L Duren, M BoehnkeAmerican Journal of Human Genetics|October 18, 2000
Strong Amerind/white sex bias and a possible Sephardic contribution among the founders of a population in northwest ColombiaL G Carvajal-Carmona, I D Soto, N Pineda, et al.American Journal of Human Genetics|October 12, 2000
Major genes regulating total serum immunoglobulin E levels in families with asthmaJ Xu, D S Postma, T D Howard, et al.American Journal of Human Genetics|April 3, 2001
The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32J P Drenth, W H Finley, G J Breedveld, et al.American Journal of Human Genetics|May 10, 2000
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform moleM V Zaragoza, U Surti, R W Redline, et al.American Journal of Human Genetics|May 10, 2000
Characterization of human crossover interferenceK W Broman, J L WeberPageof 980