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David Ravine

Showing results (11-20 of 31) with videos related to

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Annals of Family Medicine|May 14, 2014
Development and validation of a family history screening questionnaire in Australian primary careJon D Emery, Gabrielle Reid, A Toby Prevost, et al.
Human Mutation|February 20, 2004
Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndromeFranco Laccone, Ivonne Jünemann, Sharon Whatley, et al.
Lancet (London, England)|December 12, 2003
Screening for hereditary haemochromatosis within families and beyondC Anne McCune, David Ravine, Mark Worwood, et al.
Lancet (London, England)|November 1, 2005
Effectiveness of posthumous molecular diagnosis from a kept baby toothHelen Leonard, Mark R Davis, Gavin R Turbett, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Linking MECP2 and pain sensitivity: the example of Rett syndromeJenny Downs, Sandrine M Géranton, Ami Bebbington, et al.
Journal of Autism and Developmental Disorders|April 27, 2013
Brief report: do the nature of communication impairments in autism spectrum disorders relate to the broader autism phenotype in parents?Lauren J Taylor, Murray T Maybery, John Wray, et al.
Human Mutation|December 26, 2003
Large deletions in the polycystic kidney disease 1 (PKD1) geneYavuz Ariyurek, Irma Lantinga-van Leeuwen, Lia Spruit, et al.
The Journal of Pediatrics|April 18, 2006
Rett syndrome in Australia: a review of the epidemiologyCrystal L Laurvick, Nicholas de Klerk, Carol Bower, et al.
The Journal of Pediatrics|October 3, 2006
Predictors of seizure onset in Rett syndromeLe Jian, Lakshmi Nagarajan, Nicholas de Klerk, et al.
European Journal of Pediatrics|August 9, 2007
The diagnosis of autism in a female: could it be Rett syndrome?Deidra J Young, Ami Bebbington, Alison Anderson, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Annals of Family Medicine|May 14, 2014
Development and validation of a family history screening questionnaire in Australian primary careJon D Emery, Gabrielle Reid, A Toby Prevost, et al.
Human Mutation|February 20, 2004
Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndromeFranco Laccone, Ivonne Jünemann, Sharon Whatley, et al.
Lancet (London, England)|December 12, 2003
Screening for hereditary haemochromatosis within families and beyondC Anne McCune, David Ravine, Mark Worwood, et al.
Lancet (London, England)|November 1, 2005
Effectiveness of posthumous molecular diagnosis from a kept baby toothHelen Leonard, Mark R Davis, Gavin R Turbett, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Linking MECP2 and pain sensitivity: the example of Rett syndromeJenny Downs, Sandrine M Géranton, Ami Bebbington, et al.
Journal of Autism and Developmental Disorders|April 27, 2013
Brief report: do the nature of communication impairments in autism spectrum disorders relate to the broader autism phenotype in parents?Lauren J Taylor, Murray T Maybery, John Wray, et al.
Human Mutation|December 26, 2003
Large deletions in the polycystic kidney disease 1 (PKD1) geneYavuz Ariyurek, Irma Lantinga-van Leeuwen, Lia Spruit, et al.
The Journal of Pediatrics|April 18, 2006
Rett syndrome in Australia: a review of the epidemiologyCrystal L Laurvick, Nicholas de Klerk, Carol Bower, et al.
The Journal of Pediatrics|October 3, 2006
Predictors of seizure onset in Rett syndromeLe Jian, Lakshmi Nagarajan, Nicholas de Klerk, et al.
European Journal of Pediatrics|August 9, 2007
The diagnosis of autism in a female: could it be Rett syndrome?Deidra J Young, Ami Bebbington, Alison Anderson, et al.
Pageof 4