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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.
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.
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