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R J Simensen

Showing results (11-20 of 27) with videos related to

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Journal of the South Carolina Medical Association (1975)|September 1, 1982
Fragile X syndrome in South CarolinaR A Saul, R E Stevenson, R J Simensen, 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.
Journal of Medical Genetics|August 14, 2008
Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexiaF E Abidi, L Holloway, C A Moore, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X syndrome: growth, development, and intellectual functionL A Prouty, R C Rogers, R E Stevenson, et al.
American Journal of Medical Genetics|July 15, 1994
Asymmetry of methylation with FMR-1 full mutation in two 45,X/46,XX mosaic females associated with normal intellectL R Shapiro, R J Simensen, P L Wilmot, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Journal of the South Carolina Medical Association (1975)|September 1, 1982
Fragile X syndrome in South CarolinaR A Saul, R E Stevenson, R J Simensen, 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.
Journal of Medical Genetics|August 14, 2008
Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexiaF E Abidi, L Holloway, C A Moore, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X syndrome: growth, development, and intellectual functionL A Prouty, R C Rogers, R E Stevenson, et al.
American Journal of Medical Genetics|July 15, 1994
Asymmetry of methylation with FMR-1 full mutation in two 45,X/46,XX mosaic females associated with normal intellectL R Shapiro, R J Simensen, P L Wilmot, et al.
Pageof 3