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Human Heredity|April 19, 2013
Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing errorWonkuk Kim, Douglas Londono, Lisheng Zhou, et al.Pharmacogenetics|December 21, 2004
Redefinition of the human kappa opioid receptor gene (OPRK1) structure and association of haplotypes with opiate addictionVadim Yuferov, David Fussell, K Steven LaForge, et al.Journal of Human Genetics|September 9, 2016
Identification of 15 novel partial SHOX deletions and 13 partial duplications, and a review of the literature reveals intron 3 to be a hotspot regionSara Benito-Sanz, Alberta Belinchon-Martínez, Miriam Aza-Carmona, et al.Schizophrenia Research|October 3, 2008
Telomerase levels in schizophrenia: a preliminary studyBarbara Porton, Lynn E Delisi, Hilary C Bertisch, et al.BMC Proceedings|May 10, 2008
Mixture modeling of microarray gene expression dataYang Yang, Adam P Tashman, Jung Yeon Lee, et al.Neurochemical Research|March 8, 2007
Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populationsAbraham M Brown, Derek Gordon, Hsinhwa Lee, et al.Human Immunology|May 16, 2006
Disease relevant HLA class II alleles isolated by genotypic, haplotypic, and sequence analysis in North American Caucasians with pemphigus vulgarisErica Lee, Katherine A Lendas, Selwyn Chow, et al.European Journal of Human Genetics : EJHG|March 4, 2011
Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral developmentElizabeth J Bhoj, Purita Ramos, Linda A Baker, et al.Genomics|August 12, 2008
Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutationLynn Petukhova, Edilson C Sousa, Amalia Martinez-Mir, et al.Pediatric Research|February 1, 2012
IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infantsJoanna Floros, Douglas Londono, Derek Gordon, et al.Pageof 13