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American Journal of Medical Genetics. Part A
|
August 25, 2004
Fragile X syndrome phenotype with normal FMR1 gene studies
Nigel 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 review
Dimple 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 syndrome
Elizabeth 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 Syndrome
Sydney Collins, Ibrahim Bah, Ryan Pysar, et al.
Neural Plasticity
|
June 22, 2017
Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular Atrophy
Hooi 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 review
Denise 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 complex
Michael Cardamone, Danny Flanagan, David Mowat, et al.
Human Mutation
|
January 5, 2007
ZFHX1B mutations in patients with Mowat-Wilson syndrome
Florence 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 Syndrome
Justine 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 network
Lori Kiefer, John Frank, Erica Di Ruggiero, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 83) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics. Part A
|
August 25, 2004
Fragile X syndrome phenotype with normal FMR1 gene studies
Nigel 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 review
Dimple 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 syndrome
Elizabeth 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 Syndrome
Sydney Collins, Ibrahim Bah, Ryan Pysar, et al.
Neural Plasticity
|
June 22, 2017
Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular Atrophy
Hooi 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 review
Denise 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 complex
Michael Cardamone, Danny Flanagan, David Mowat, et al.
Human Mutation
|
January 5, 2007
ZFHX1B mutations in patients with Mowat-Wilson syndrome
Florence 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 Syndrome
Justine 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 network
Lori Kiefer, John Frank, Erica Di Ruggiero, et al.
Page
of 9