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Birth Defects Research. Part A, Clinical and Molecular Teratology|March 18, 2014
Nonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in YemenKhalid Ahmed Aldhorae, Anne C Böhmer, Kerstin U Ludwig, et al.
Translational Psychiatry|July 12, 2012
Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spellingJ Becker, D Czamara, P Hoffmann, et al.
European Journal of Human Genetics : EJHG|May 28, 2009
A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patientsHartmut Engels, Eva Wohlleber, Alexander Zink, 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.
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.
Kidney International|January 21, 2026
Sodium glucose transporter 2 inhibition maintains kidney antibacterial response by decreasing complement C1qGeorg W Sendtner, Julia Miranda, Pia Naumann, 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.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 25, 2010
Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21Inke R König, Johannes Schumacher, Per Hoffmann, et al.
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