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Human Heredity|April 19, 2013
Rare variants in complex traits: novel identification strategies and the role of de novo mutationsLoubna Jouan, Julie Gauthier, Patrick A Dion, et al.Human Heredity|January 1, 1990
Is there a sex-phenotype association for esterase D (EC 3.1.1.1)?A M Moro-Furlani, P H Cabello, H KriegerHuman Heredity|January 1, 1990
A genetic study of immunoglobulin E and atopic disease based on families ascertained through asthmatic childrenT Parks, K Felix, T Rice, et al.Human Heredity|January 1, 1990
Partial trisomy of chromosome 18 (pter----q12) following a familial 18;21 translocation rcp(18;21)(q12;q11)F Binkert, J Stranzinger, A SchinzelHuman Heredity|July 26, 2014
Population-genetic influences on genomic estimates of the inbreeding coefficient: a global perspectiveTrevor J Pemberton, Noah A RosenbergHuman Heredity|July 26, 2014
Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studiesTommaso Pippucci, Alberto Magi, Alessandro Gialluisi, et al.Human Heredity|July 26, 2014
Consanguinity and disorders of sex developmentAnu Bashamboo, Ken McElreaveyHuman Heredity|July 26, 2014
The use of autozygosity mapping and next-generation sequencing in understanding anterior segment defects caused by an abnormal development of the lensRachel L Gillespie, I Christopher Lloyd, Graeme C M BlackHuman Heredity|July 26, 2014
Incorporating gene-environment interaction in testing for association with rare genetic variantsHan Chen, James B Meigs, Josée DupuisPageof 237