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Richard Simensen

Showing results (1-10 of 9) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 22, 2008
Cognitive-behavioral features of children with Wolf-Hirschhorn syndrome: preliminary report of 12 casesGene S Fisch, Agatino Battaglia, Barbara Parrini, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 29, 2010
Cognitive-behavioral features of Wolf-Hirschhorn syndrome and other subtelomeric microdeletionsGene S Fisch, Paul Grossfeld, Rena Falk, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
The course of cognitive-behavioral development in children with the FMR1 mutation, Williams-Beuren syndrome, and neurofibromatosis type 1: The effect of genderGene S Fisch, Nancy Carpenter, Patricia N Howard-Peebles, et al.
JIMD Reports|November 20, 2019
Intellectual functioning in alpha-mannosidosisSara S Cathey, Sara M Sarasua, Richard Simensen, et al.
American Journal on Intellectual and Developmental Disabilities|April 21, 2012
Developmental trajectories in syndromes with intellectual disability, with a focus on Wolf-Hirschhorn and its cognitive-behavioral profileGene S Fisch, Nancy Carpenter, Patricia N Howard-Peebles, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
Studies of age-correlated features of cognitive-behavioral development in children and adolescents with genetic disordersGene S Fisch, Nancy Carpenter, Patricia N Howard-Peebles, et al.
American Journal of Medical Genetics. Part A|April 13, 2011
Deletion of the immunoglobulin domain of IL1RAPL1 results in nonsyndromic X-linked intellectual disability associated with behavioral problems and mild dysmorphismKarl J Franek, Julia Butler, John Johnson, et al.
Pediatrics|November 8, 2006
Recurrent infections, hypotonia, and mental retardation caused by duplication of MECP2 and adjacent region in Xq28Michael J Friez, Julie R Jones, Katie Clarkson, et al.
American Journal of Medical Genetics. Part A|November 1, 2008
Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p.R961W mutation in the MED12 geneJohn M Graham, Jeannie Visootsak, Elisabeth Dykens, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 22, 2008
Cognitive-behavioral features of children with Wolf-Hirschhorn syndrome: preliminary report of 12 casesGene S Fisch, Agatino Battaglia, Barbara Parrini, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 29, 2010
Cognitive-behavioral features of Wolf-Hirschhorn syndrome and other subtelomeric microdeletionsGene S Fisch, Paul Grossfeld, Rena Falk, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
The course of cognitive-behavioral development in children with the FMR1 mutation, Williams-Beuren syndrome, and neurofibromatosis type 1: The effect of genderGene S Fisch, Nancy Carpenter, Patricia N Howard-Peebles, et al.
JIMD Reports|November 20, 2019
Intellectual functioning in alpha-mannosidosisSara S Cathey, Sara M Sarasua, Richard Simensen, et al.
American Journal on Intellectual and Developmental Disabilities|April 21, 2012
Developmental trajectories in syndromes with intellectual disability, with a focus on Wolf-Hirschhorn and its cognitive-behavioral profileGene S Fisch, Nancy Carpenter, Patricia N Howard-Peebles, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
Studies of age-correlated features of cognitive-behavioral development in children and adolescents with genetic disordersGene S Fisch, Nancy Carpenter, Patricia N Howard-Peebles, et al.
American Journal of Medical Genetics. Part A|April 13, 2011
Deletion of the immunoglobulin domain of IL1RAPL1 results in nonsyndromic X-linked intellectual disability associated with behavioral problems and mild dysmorphismKarl J Franek, Julia Butler, John Johnson, et al.
Pediatrics|November 8, 2006
Recurrent infections, hypotonia, and mental retardation caused by duplication of MECP2 and adjacent region in Xq28Michael J Friez, Julie R Jones, Katie Clarkson, et al.
American Journal of Medical Genetics. Part A|November 1, 2008
Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p.R961W mutation in the MED12 geneJohn M Graham, Jeannie Visootsak, Elisabeth Dykens, et al.
Pageof 1