Showing results (161-170 of 238) with videos related to

Sort By:
Pageof 24
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.
American Journal of Medical Genetics. Part A|September 17, 2013
Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sampleAnne C Böhmer, Elisabeth Mangold, Peter Tessmann, et al.
Clinical Genetics|September 20, 2017
Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palateA Mostowska, A Gaczkowska, K Żukowski, et al.
HGG Advances|January 20, 2022
Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palateJulia Welzenbach, Nigel L Hammond, Miloš Nikolić, et al.
HGG Advances|January 2, 2023
Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutationsHanna K Zieger, Leonie Weinhold, Axel Schmidt, et al.
Psychiatric Genetics|November 20, 2008
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sampleKerstin U Ludwig, Johannes Schumacher, Gerd Schulte-Körne, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 8, 2014
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathwayTaofik Al Chawa, Kerstin U Ludwig, Heide Fier, et al.
NPJ Genomic Medicine|July 2, 2021
TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19Axel Schmidt, Sophia Peters, Alexej Knaus, et al.
International Journal of Pediatric Otorhinolaryngology|November 4, 2010
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patientsNilma Almeida de Assis, Stefanie Nowak, Kerstin U Ludwig, et al.
American Journal of Medical Genetics. Part A|February 28, 2012
A phenotype map for 14q32.3 terminal deletionsHartmut Engels, Herdit M Schüler, Alexander M Zink, et al.
Pageof 24