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European Journal of Medical Genetics|June 3, 2006
Detection of a deletion of exons 8-16 of the UBE3A gene in familial Angelman syndrome using a semi-quantitative dosage PCR based assayL Boyes, A J Wallace, M Krajewska-Walasek, et al.
Clinical Dysmorphology|July 6, 2019
Traboulsi syndrome due to ASPH mutation: an under-recognised cause of ectopia lentisNainesha Kulkarni, Ian C Lloyd, Jane Ashworth, et al.
Ophthalmic Genetics|October 27, 2009
Microcephaly with chorioretinal dysplasia: two case reports and a review of the literatureAbha Gupta, P Vasudevan, S Biswas, et al.
British Dental Journal|December 9, 1989
The visibility of clear and opaque fissure sealantsW P Rock, A J Potts, M D Marchment, et al.
American Journal of Medical Genetics. Part A|November 4, 2004
Symptomatic Chiari I malformation in Kabuki syndromeKaren L Ciprero, Jill Clayton-Smith, Dian Donnai, et al.
Research in Comparative and International Education|February 23, 2026
Educator and student perspectives for enhancing international students' sense of belonging in Ontario secondary schoolsClayton Smith, George Zhou, Thu Thi Kim Le, et al.
Journal of Medical Genetics|July 1, 1989
Testing for cystic fibrosis using allelic associationA J Ivinson, A P Read, R Harris, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 12, 2008
Folate and clefts of the lip and palate--a U.K.-based case-control study: Part I: Dietary and supplemental folateJ Little, M Gilmour, P A Mossey, et al.
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