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European Journal of Medical Genetics|July 17, 2012
Interpretation of clinical relevance of X-chromosome copy number variations identified in a large cohort of individuals with cognitive disorders and/or congenital anomaliesMarjolein H Willemsen, Nicole de Leeuw, Arjan P M de Brouwer, et al.
European Journal of Medical Genetics|March 21, 2009
The 12q14 microdeletion syndrome: additional patients and further evidence that HMGA2 is an important genetic determinant for human heightKaren Buysse, William Reardon, Lakshmi Mehta, et al.
Rheumatology (Oxford, England)|September 29, 1999
The depletion of T cells from haematopoietic stem cell transplantsI C Slaper-Cortenbach, M J Wijngaarden-du Bois, A de Vries-van Rossen, et al.
Clinical Genetics|September 19, 2008
A clinical and genetic study of the Say/Barber/Biesecker/Young-Simpson type of Ohdo syndromeR Day, B Beckett, D Donnai, et al.
European Journal of Human Genetics : EJHG|September 10, 2015
Novel genetic causes for cerebral visual impairmentDaniëlle G M Bosch, F Nienke Boonstra, Nicole de Leeuw, et al.
Atherosclerosis|February 27, 2018
Progression of subclinical atherosclerosis in subjects with rheumatoid arthritis and the metabolic syndromeBenjamin Burggraaf, Deborah F van Breukelen-van der Stoep, Marijke A de Vries, et al.
The American Journal of Gastroenterology|July 9, 2009
Early HBeAg loss during peginterferon alpha-2b therapy predicts HBsAg loss: results of a long-term follow-up study in chronic hepatitis B patientsErik H C J Buster, Hajo J Flink, Halis Simsek, et al.
Journal of Clinical Microbiology|February 4, 2011
Chronic Q fever-related dual-pathogen endocarditis: case series of three patientsLinda M Kampschreur, Jan Jelrik Oosterheert, Cornelia A de Vries Feyens, et al.
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