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Journal of Medical Genetics|October 3, 1999
A new gene (DYX3) for dyslexia is located on chromosome 2T Fagerheim, P Raeymaekers, F E Tønnessen, et al.Current Opinion in Pediatrics|May 24, 2011
Supraclavicular swelling in hypothyroidismScott A Clements, Sharon H TraversCJEM|September 24, 2016
Contemporary evidence-based practice in Canadian emergency medical services: a vision for integrating evidence into clinical and policy decision-makingJan L Jensen, Andrew H TraversScience (New York, N.Y.)|July 24, 1970
Genetic polymorphisms of human mitochondrial glutamic oxaloacetic transaminaseR G Davidson, J A Cortner, M C Rattazzi, et al.British Journal of Urology|December 1, 1993
Development of hydronephrosis in spina bifida patients: predictive factors and managementP A Anderson, A H TraversAnnales De Genetique|December 11, 1976
Duplication-deficiency of the short arm of chromosome 8 following artificial inseminationR G Weleber, R S Verma, W J Kimberling, et al.Muscle & Nerve|July 1, 1978
Late-onset X-linked recessive spinal and bulbar muscular atrophyS P Ringel, N S Lava, M M Treihaft, et al.Clinical Genetics|April 10, 2002
Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 geneR R Lebel, M May, S Pouls, et al.Clinical Genetics|October 1, 1996
Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21B Häne, R J Schroer, J F Arena, et al.American Journal of Medical Genetics|July 9, 1999
Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22B Häne, R E Stevenson, J F Arena, et al.Pageof 15