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Human Mutation|June 18, 2009
Deletions in the VPS13B (COH1) gene as a cause of Cohen syndromeI Balikova, A-E Lehesjoki, T J L de Ravel, et al.
Immunome Research|November 25, 2005
AntiJen: a quantitative immunology database integrating functional, thermodynamic, kinetic, biophysical, and cellular dataChristopher P Toseland, Debra J Clayton, Helen McSparron, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutationsR Perveen, I C Lloyd, J Clayton-Smith, 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 II: Biochemical and genetic analysisJ Little, M Gilmour, P A Mossey, et al.
Archives of Neurology|December 1, 1985
Neurologic signs in senescenceL R Jenkyn, A G Reeves, T Warren, et al.
Journal of Affective Disorders|April 26, 2006
The distinct temperament profiles of bipolar I, bipolar II and unipolar patientsHagop S Akiskal, Nael Kilzieh, Jack D Maser, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 16, 2025
Cardiovascular function in people with cystic fibrosis on Elexacaftor/Tezacaftor/Ivacaftor: A cross-sectional, observational, single-centre studyLauren J Clayton, Anthony I Shepherd, Jo Corbett, et al.
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