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Pediatric Research|April 21, 2017
Association of candidate gene polymorphisms with clinical subtypes of preterm birth in a Latin American populationLucas G Gimenez, Allison M Momany, Fernando A Poletta, et al.Innate Immunity|October 11, 2013
Identification of single nucleotide polymorphisms in hematopoietic cell transplant patients affecting early recognition of, and response to, endotoxinEva C Guinan, Christine D Palmer, Christy J Mancuso, et al.Plos Medicine|January 28, 2014
A risk prediction model for the assessment and triage of women with hypertensive disorders of pregnancy in low-resourced settings: the miniPIERS (Pre-eclampsia Integrated Estimate of RiSk) multi-country prospective cohort studyBeth A Payne, Jennifer A Hutcheon, J Mark Ansermino, et al.Bulletin of the World Health Organization|April 30, 2010
Tracking maternal mortality declines in Mongolia between 1992 and 2007: the importance of collaborationBuyanjargal Yadamsuren, Mario Merialdi, Ishnyam Davaadorj, et al.Science Translational Medicine|June 8, 2012
Noninvasive whole-genome sequencing of a human fetusJacob O Kitzman, Matthew W Snyder, Mario Ventura, et al.Plos One|August 13, 2013
A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial cleftingAdam P Ross, M Adela Mansilla, Youngshik Choe, et al.Journal of Medical Genetics|April 14, 2012
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleUppala Radhakrishna, Swapan K Nath, Ken McElreavey, et al.Genetic Epidemiology|December 3, 2016
Whole exome association of rare deletions in multiplex oral cleft familiesJack Fu, Terri H Beaty, Alan F Scott, et al.Plos One|April 25, 2013
X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association studySolveig Myking, Heather A Boyd, Ronny Myhre, et al.American Journal of Human Genetics|December 27, 2011
Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locusKaren Mitchell, James O'Sullivan, Caterina Missero, et al.Pageof 43