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Reproductive Sciences (Thousand Oaks, Calif.)|January 27, 2011
Single-nucleotide polymorphisms in the KCNN3 gene associate with preterm birthLori J Day, Kendra L Schaa, Kelli K Ryckman, et al.
JAMA|August 31, 2013
Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosisBjarke Feenstra, Frank Geller, Lisbeth Carstensen, et al.
Annals of Plastic Surgery|April 28, 2006
Candidate genes for oral-facial clefts in Guatemalan familiesKatherine Neiswanger, Frederic W B Deleyiannis, Joseph R Avila, et al.
BMC Health Services Research|June 3, 2014
Implementation of evidence-based antenatal care in Mozambique: a cluster randomized controlled trial: study protocolLeonardo Chavane, Mario Merialdi, Ana Pilar Betrán, et al.
BMC Pregnancy and Childbirth|June 3, 2014
WHO multicentre study for the development of growth standards from fetal life to childhood: the fetal componentMario Merialdi, Mariana Widmer, Ahmet Metin Gülmezoglu, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2007
Impaired FGF signaling contributes to cleft lip and palateBridget M Riley, M Adela Mansilla, Jinghong Ma, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 10, 2004
In a Vietnamese population, MSX1 variants contribute to cleft lip and palateYasushi Suzuki, Peter A Jezewski, Junichiro Machida, et al.
European Journal of Human Genetics : EJHG|May 10, 2012
PITX2 and FOXC1 spectrum of mutations in ocular syndromesLinda M Reis, Rebecca C Tyler, Bethany A Volkmann Kloss, et al.
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