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David Mowat

Showing results (11-20 of 83) with videos related to

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American Journal of Medical Genetics. Part A|August 25, 2004
Fragile X syndrome phenotype with normal FMR1 gene studiesNigel F Clarke, David Mowat, R Frank Kooy, et al.
Journal of Paediatrics and Child Health|July 22, 2016
FOXF1 gene mutation in alveolar capillary dysplasia associated with Hirschsprung's disease and clinical reviewDimple Goel, Ju Lee Oei, Antonia W Shand, et al.
American Journal of Medical Genetics. Part A|January 17, 2012
The behavioral phenotype of Mowat-Wilson syndromeElizabeth Evans, Stewart Einfeld, David Mowat, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Whole Genome Sequencing Reveals a <i>RET</i> Enhancer Risk Haplotype Associated with Hirschsprung Disease in Mowat Wilson SyndromeSydney Collins, Ibrahim Bah, Ryan Pysar, et al.
Neural Plasticity|June 22, 2017
Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular AtrophyHooi Ling Teoh, Kate Carey, Hugo Sampaio, et al.
Reviews in the Neurosciences|December 7, 2017
The natural history of subependymal giant cell astrocytomas in tuberous sclerosis complex: a reviewDenise L Chan, Tessa Calder, John A Lawson, et al.
The Journal of Pediatrics|February 13, 2014
Mammalian target of rapamycin inhibitors for intractable epilepsy and subependymal giant cell astrocytomas in tuberous sclerosis complexMichael Cardamone, Danny Flanagan, David Mowat, et al.
Human Mutation|January 5, 2007
ZFHX1B mutations in patients with Mowat-Wilson syndromeFlorence Dastot-Le Moal, Meredith Wilson, David Mowat, et al.
Research in Developmental Disabilities|January 18, 2017
Incontinence and psychological symptoms in individuals with Mowat-Wilson SyndromeJustine Niemczyk, Stewart Einfeld, David Mowat, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|May 26, 2005
Fostering evidence-based decision-making in Canada: examining the need for a Canadian population and public health evidence centre and research networkLori Kiefer, John Frank, Erica Di Ruggiero, et al.
Pageof 9

Showing results (11-20 of 83) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics. Part A|August 25, 2004
Fragile X syndrome phenotype with normal FMR1 gene studiesNigel F Clarke, David Mowat, R Frank Kooy, et al.
Journal of Paediatrics and Child Health|July 22, 2016
FOXF1 gene mutation in alveolar capillary dysplasia associated with Hirschsprung's disease and clinical reviewDimple Goel, Ju Lee Oei, Antonia W Shand, et al.
American Journal of Medical Genetics. Part A|January 17, 2012
The behavioral phenotype of Mowat-Wilson syndromeElizabeth Evans, Stewart Einfeld, David Mowat, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Whole Genome Sequencing Reveals a <i>RET</i> Enhancer Risk Haplotype Associated with Hirschsprung Disease in Mowat Wilson SyndromeSydney Collins, Ibrahim Bah, Ryan Pysar, et al.
Neural Plasticity|June 22, 2017
Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular AtrophyHooi Ling Teoh, Kate Carey, Hugo Sampaio, et al.
Reviews in the Neurosciences|December 7, 2017
The natural history of subependymal giant cell astrocytomas in tuberous sclerosis complex: a reviewDenise L Chan, Tessa Calder, John A Lawson, et al.
The Journal of Pediatrics|February 13, 2014
Mammalian target of rapamycin inhibitors for intractable epilepsy and subependymal giant cell astrocytomas in tuberous sclerosis complexMichael Cardamone, Danny Flanagan, David Mowat, et al.
Human Mutation|January 5, 2007
ZFHX1B mutations in patients with Mowat-Wilson syndromeFlorence Dastot-Le Moal, Meredith Wilson, David Mowat, et al.
Research in Developmental Disabilities|January 18, 2017
Incontinence and psychological symptoms in individuals with Mowat-Wilson SyndromeJustine Niemczyk, Stewart Einfeld, David Mowat, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|May 26, 2005
Fostering evidence-based decision-making in Canada: examining the need for a Canadian population and public health evidence centre and research networkLori Kiefer, John Frank, Erica Di Ruggiero, et al.
Pageof 9