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Genetic Counseling (Geneva, Switzerland)|October 28, 2003
A prenatal counseling conundrum: mosaic trisomy 16. A case study presenting cognitive functioning and adaptive behaviorR J Simensen, R S Colby, K J CorningAmerican Journal of Mental Deficiency|March 1, 1987
Fragile X syndrome: a common etiology of mental retardationR C Rogers, R J SimensenClinical Genetics|May 29, 2002
Cognitive function in Coffin-Lowry syndromeR J Simensen, F Abidi, J S Collins, et al.Genetic Counseling (Geneva, Switzerland)|May 23, 2012
Short-term memory deficits in carrier females with KDM5C mutationsR J Simensen, R C Rogers, J S Collins, 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.Clinical Genetics|July 1, 1980
Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6R J Schroer, D M Culp, R E Stevenson, et al.American Journal of Human Genetics|September 1, 1990
Allan-Herndon syndrome. I. Clinical studiesR E Stevenson, H O Goodman, C E Schwartz, et al.American Journal of Medical Genetics|January 2, 1995
Deletion involving D15S113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion regionR C Michaelis, S A Skinner, B A Lethco, et al.Journal of Medical Genetics|July 21, 2009
Phenotype and genotype in mucolipidoses II and III alpha/beta: a study of 61 probandsS S Cathey, J G Leroy, T Wood, et al.Pageof 2