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Journal of Human Genetics|November 18, 2003
Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletionShuji Kayano, Shigeo Kure, Yoichi Suzuki, et al.
Thescientificworldjournal|March 28, 2013
Genome-wide analysis of DNA methylation in human amnionJinsil Kim, Mitchell M Pitlick, Paul J Christine, et al.
Genesis (New York, N.Y. : 2000)|September 12, 2020
Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disordersBrent H Wyatt, Thomas O Raymond, Lisa A Lansdon, et al.
Biological Research for Nursing|April 18, 2017
Relationship of Genetic Variants With Procedural Pain, Anxiety, and Distress in ChildrenAnne L Ersig, Debra L Schutte, Jennifer Standley, et al.
Genetic Epidemiology|March 26, 2003
Variants of developmental genes (TGFA, TGFB3, and MSX1) and their associations with orofacial clefts: a case-parent triad analysisAstanand Jugessur, Rolv T Lie, Allen J Wilcox, et al.
American Journal of Obstetrics and Gynecology|August 11, 2007
Blood pressure dynamics during pregnancy and spontaneous preterm birthJun Zhang, Jose Villar, Wenyu Sun, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|October 28, 2011
Biomarkers of spontaneous preterm birth: an overview of the literature in the last four decadesRamkumar Menon, Maria Regina Torloni, Chiara Voltolini, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 3, 2004
Analysis of two translocation breakpoints and identification of a negative regulatory element in patients with Rieger's syndromeDimitri G Trembath, Elena V Semina, Douglas H Jones, et al.
Human Biology|October 6, 2005
Dermatoglyphic fingerprint heterogeneity among individuals with nonsyndromic cleft lip with or without cleft palate and their unaffected relatives in China and the PhilippinesNicole M Scott, Seth M Weinberg, Katherine Neiswanger, et al.
American Journal of Perinatology|November 8, 2012
Environmental risk factors and perinatal outcomes in preterm newborns, according to family recurrence of prematurityHugo B Krupitzki, Enrique C Gadow, Juan A Gili, et al.
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