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Statistical Applications in Genetics and Molecular Biology|May 2, 2006
Computing asymptotic power and sample size for case-control genetic association studies in the presence of phenotype and/or genotype misclassification errorsFei Ji, Yaning Yang, Chad Haynes, et al.
European Journal of Human Genetics : EJHG|April 9, 2002
Second family with hearing impairment linked to 19q13 and refined DFNA4 localisationFarhad Mirghomizadeh, Bettina Bardtke, Marcella Devoto, et al.
Human Mutation|March 14, 2015
Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresiaEllen A Tsai, Christopher M Grochowski, Alexandra M Falsey, et al.
European Journal of Human Genetics : EJHG|April 14, 2005
Univariate and bivariate variance component linkage analysis of a whole-genome scan for loci contributing to bone mineral densityMarcella Devoto, Loretta D Spotila, Deborah L Stabley, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 14, 2016
IQ and hemizygosity for the Val158 Met functional polymorphism of COMT in 22q11DSColleen P Franconi, Donna McDonald-McGinn, Elaine H Zackai, et al.
The Journal of Investigative Dermatology. Symposium Proceedings|October 30, 2003
Genetic linkage studies in alopecia areataAmalia Martinez-Mir, Abraham Zlotogorski, Jurg Ott, et al.
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