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Wendy H Raskind

Showing results (1-10 of 82) with videos related to

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Topics in Language Disorders|September 13, 2011
A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtypeBeate Peter, Wendy H Raskind
Psychiatric Genetics|April 21, 2012
Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational familyBeate Peter, Mark Matsushita, Wendy H Raskind
Journal of Speech, Language, and Hearing Research : JSLHR|November 18, 2010
Global processing speed in children with low reading ability and in children and adults with typical reading ability: exploratory factor analytic modelsBeate Peter, Mark Matsushita, Wendy H Raskind
Personalized Medicine|September 4, 2009
Pharmacology and genetics of autism: implications for diagnosis and treatmentZoran Brkanac, Wendy H Raskind, Bryan H King
The Lancet. Oncology|November 8, 2016
Biochemical and imaging surveillance in Li-Fraumeni syndromeWendy H Raskind, Fuki M Hisama, Robin L Bennett
Gene|October 22, 2008
Human phenotypes associated with GATA-1 mutationsWendy A Ciovacco, Wendy H Raskind, Melissa A Kacena
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 14Dong-Hui Chen, Wendy H Raskind, Thomas D Bird
Clinical Linguistics & Phonetics|January 24, 2013
Associations among measures of sequential processing in motor and linguistics tasks in adults with and without a family history of childhood apraxia of speech: a replication studyLe Button, Beate Peter, Carol Stoel-Gammon, et al.
Seminars in Thrombosis and Hemostasis|November 22, 2011
Inherited thrombocytopenia due to GATA-1 mutationsPatrick D Millikan, Sanjeev M Balamohan, Wendy H Raskind, et al.
American Journal of Medical Genetics. Part A|June 17, 2008
Sensorineural deafness, distinctive facial features, and abnormal cranial bones: a new variant of Waardenburg syndrome?Alona Gad, Mercy Laurino, Kenneth R Maravilla, et al.
Pageof 9

Showing results (1-10 of 82) with videos related to

Sort By:
Pageof 9
Topics in Language Disorders|September 13, 2011
A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtypeBeate Peter, Wendy H Raskind
Psychiatric Genetics|April 21, 2012
Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational familyBeate Peter, Mark Matsushita, Wendy H Raskind
Journal of Speech, Language, and Hearing Research : JSLHR|November 18, 2010
Global processing speed in children with low reading ability and in children and adults with typical reading ability: exploratory factor analytic modelsBeate Peter, Mark Matsushita, Wendy H Raskind
Personalized Medicine|September 4, 2009
Pharmacology and genetics of autism: implications for diagnosis and treatmentZoran Brkanac, Wendy H Raskind, Bryan H King
The Lancet. Oncology|November 8, 2016
Biochemical and imaging surveillance in Li-Fraumeni syndromeWendy H Raskind, Fuki M Hisama, Robin L Bennett
Gene|October 22, 2008
Human phenotypes associated with GATA-1 mutationsWendy A Ciovacco, Wendy H Raskind, Melissa A Kacena
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 14Dong-Hui Chen, Wendy H Raskind, Thomas D Bird
Clinical Linguistics & Phonetics|January 24, 2013
Associations among measures of sequential processing in motor and linguistics tasks in adults with and without a family history of childhood apraxia of speech: a replication studyLe Button, Beate Peter, Carol Stoel-Gammon, et al.
Seminars in Thrombosis and Hemostasis|November 22, 2011
Inherited thrombocytopenia due to GATA-1 mutationsPatrick D Millikan, Sanjeev M Balamohan, Wendy H Raskind, et al.
American Journal of Medical Genetics. Part A|June 17, 2008
Sensorineural deafness, distinctive facial features, and abnormal cranial bones: a new variant of Waardenburg syndrome?Alona Gad, Mercy Laurino, Kenneth R Maravilla, et al.
Pageof 9