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Journal of Dental Research|July 22, 2017
The Role of Noncoding Genetic Variation in Isolated Orofacial CleftsF Thieme, K U LudwigThe British Journal of Dermatology|May 25, 2013
Evidence for a polygenic contribution to androgenetic alopeciaS Heilmann, F F Brockschmidt, A M Hillmer, et al.Molecular Psychiatry|September 30, 2009
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic childrenD Roeske, K U Ludwig, N Neuhoff, 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.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.Human Genetics|March 21, 2013
Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio studyT H Beaty, M A Taub, A F Scott, et al.Translational Psychiatry|February 21, 2013
A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adultsK U Ludwig, P Sämann, M Alexander, et al.Journal of Dental Research|September 16, 2021
MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell MigrationL G Stüssel, R Hollstein, M Laugsch, et al.Journal of Dental Research|October 21, 2017
MRPL53, a New Candidate Gene for Orofacial Clefting, Identified Using an eQTL ApproachC Masotti, L A Brito, A C Nica, et al.Journal of Dental Research|February 25, 2014
Strong association of variants around FOXE1 and orofacial cleftingK U Ludwig, A C Böhmer, M Rubini, et al.Pageof 2