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Human Molecular Genetics|October 26, 2005
Identification of disease genes by whole genome CGH arraysLisenka E L M Vissers, Joris A Veltman, Ad Geurts van Kessel, et al.Biological Psychiatry|July 20, 2010
Genetic variation in CACNA1C, a gene associated with bipolar disorder, influences brainstem rather than gray matter volume in healthy individualsBarbara Franke, Alejandro Arias Vasquez, Joris A Veltman, et al.American Journal of Medical Genetics|April 24, 1999
Craniosynostosis associated with ectopia lentis in monozygotic twin sistersJ R Cruysberg, C M van Ravenswaaij-Arts, A Pinckers, et al.European Journal of Human Genetics : EJHG|February 24, 2006
A text-mining analysis of the human phenomeMarc A van Driel, Jorn Bruggeman, Gert Vriend, et al.Annales De Genetique|May 4, 2001
The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR)G J Van Buggenhout, J C Trommelen, H G Brunner, et al.European Journal of Clinical Investigation|August 1, 1995
Four week administration of an ACE inhibitor and a cardioselective beta-blocker in healthy volunteers: no influence on insulin sensitivityL Heinemann, T Heise, J Ampudia, et al.Journal of Genetic Counseling|November 11, 2022
Clinical geneticists' views on and experiences with unsolicited findings in next-generation sequencing: "A great technology creating new dilemmas"Vyne van der Schoot, Carlijn Damsté, Helger G Yntema, et al.Neurobiology of Aging|July 6, 2011
CR1 genotype is associated with entorhinal cortex volume in young healthy adultsJanita Bralten, Barbara Franke, Alejandro Arias-Vásquez, et al.Journal of Neural Transmission. Supplementum|June 13, 1998
Monoamine oxidase A deficiency: biogenic amine metabolites in random urine samplesN G Abeling, A H van Gennip, A G van Cruchten, et al.The Journal of Clinical Endocrinology and Metabolism|June 18, 1999
Analysis of mutations in genes of the follicle-stimulating hormone receptor signaling pathway in ovarian granulosa cell tumorsM J Ligtenberg, M Siers, A P Themmen, et al.Pageof 73