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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|May 3, 2008
Family-based association study of the MTHFR polymorphism C677T in patients with nonsyndromic cleft lip and palate from central EuropeHeiko Reutter, Stefanie Birnbaum, Amalia Diaz Lacava, et al.Human Molecular Genetics|October 11, 2025
Genetic heterogeneity and homogeneity among orofacial cleft subtypes: genome-wide association studies in the cleft collectiveKyle Dack, Kerstin U Ludwig, Evie Stergiakouli, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|January 3, 2014
Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican populationKerstin U Ludwig, Philipp Wahle, Heiko Reutter, et al.Psychiatric Genetics|March 9, 2017
Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxietyAndreas J Forstner, Stefanie Rambau, Nina Friedrich, et al.Investigative Ophthalmology & Visual Science|January 1, 2016
Monoallelic ABCA4 Mutations Appear Insufficient to Cause Retinopathy: A Quantitative Autofluorescence StudyPhilipp L Müller, Martin Gliem, Elisabeth Mangold, et al.Cancer Letters|January 17, 2007
The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1Stefan Krüger, Christoph Engel, Andrea Bier, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|July 8, 2016
Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palateJohanna Klamt, Andrea Hofmann, Anne C Böhmer, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 29, 2025
KLHL13 functional defects cause neurodevelopmental disorder in humans that can be rescued via inhibition of AURKB in cellular and animal modelsTehmeena Akhter, Zubair M Ahmed, Yaping Ji, et al.Journal of Human Genetics|May 16, 2008
TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palateHeiko Reutter, Stefanie Birnbaum, Meinhard Mende, et al.Human Molecular Genetics|June 21, 2026
Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrixJulia A Capecki, Helena Shkuro, Öznur Yilmaz, et al.Pageof 14