Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Oliver W J Quarrell

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
Clinical Dysmorphology|March 14, 2007
Prader-Willi and Klinefelter syndrome: a coincidence or not?Pradeep C Vasudevan, Oliver W J Quarrell
Clinical Dysmorphology|November 6, 2025
Observed total and live birth prevalence of Wolf-Hirschhorn syndrome in England 2015-2020Oliver W J Quarrell, Ewoma Obaro, Alexander Thompson, et al.
Prenatal Diagnosis|February 2, 2006
The OEIS complex: two case reports that illustrate the spectrum of abnormalities and a review of the literaturePradeep C Vasudevan, Marta C Cohen, Elspeth H Whitby, et al.
Neurodegenerative Disease Management|January 14, 2014
Managing juvenile Huntington's diseaseOliver W J Quarrell, Martha A Nance, Peggy Nopoulos, et al.
Journal of Child Health Care : for Professionals Working with Children in the Hospital and Community|February 9, 2007
Caring for a child with Juvenile Huntington's Disease: helpful and unhelpful supportHelen M Brewer, Jonathan A Smith, Virginia Eatough, et al.
Journal of Health Psychology|December 19, 2007
The impact of Juvenile Huntington's Disease on the family: the case of a rare childhood conditionHelen M Brewer, Virginia Eatough, Jonathan A Smith, et al.
Clinical Dysmorphology|June 3, 2005
Microcephaly-lymphoedema-chorioretinal dysplasia: three cases to delineate the facial phenotype and review of the literaturePradeep C Vasudevan, Sixto Garcia-Minaur, Maria Pilar Botella, et al.
European Journal of Human Genetics : EJHG|April 28, 2006
Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic herniaPradeep C Vasudevan, Stephen R F Twigg, John B Mulliken, et al.
European Journal of Human Genetics : EJHG|March 17, 2005
Genetic professionals' reports of nondisclosure of genetic risk information within familiesAngus Clarke, Martin Richards, Lauren Kerzin-Storrar, et al.
Journal of Medical Genetics|March 16, 2007
Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational studyOliver W J Quarrell, Alan S Rigby, L Barron, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Clinical Dysmorphology|March 14, 2007
Prader-Willi and Klinefelter syndrome: a coincidence or not?Pradeep C Vasudevan, Oliver W J Quarrell
Clinical Dysmorphology|November 6, 2025
Observed total and live birth prevalence of Wolf-Hirschhorn syndrome in England 2015-2020Oliver W J Quarrell, Ewoma Obaro, Alexander Thompson, et al.
Prenatal Diagnosis|February 2, 2006
The OEIS complex: two case reports that illustrate the spectrum of abnormalities and a review of the literaturePradeep C Vasudevan, Marta C Cohen, Elspeth H Whitby, et al.
Neurodegenerative Disease Management|January 14, 2014
Managing juvenile Huntington's diseaseOliver W J Quarrell, Martha A Nance, Peggy Nopoulos, et al.
Journal of Child Health Care : for Professionals Working with Children in the Hospital and Community|February 9, 2007
Caring for a child with Juvenile Huntington's Disease: helpful and unhelpful supportHelen M Brewer, Jonathan A Smith, Virginia Eatough, et al.
Journal of Health Psychology|December 19, 2007
The impact of Juvenile Huntington's Disease on the family: the case of a rare childhood conditionHelen M Brewer, Virginia Eatough, Jonathan A Smith, et al.
Clinical Dysmorphology|June 3, 2005
Microcephaly-lymphoedema-chorioretinal dysplasia: three cases to delineate the facial phenotype and review of the literaturePradeep C Vasudevan, Sixto Garcia-Minaur, Maria Pilar Botella, et al.
European Journal of Human Genetics : EJHG|April 28, 2006
Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic herniaPradeep C Vasudevan, Stephen R F Twigg, John B Mulliken, et al.
European Journal of Human Genetics : EJHG|March 17, 2005
Genetic professionals' reports of nondisclosure of genetic risk information within familiesAngus Clarke, Martin Richards, Lauren Kerzin-Storrar, et al.
Journal of Medical Genetics|March 16, 2007
Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational studyOliver W J Quarrell, Alan S Rigby, L Barron, et al.
Pageof 2