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Elisabeth Rosser

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European Journal of Cancer (Oxford, England : 1990)|November 3, 2004
Inherited cancer in children: practical/ethical problems and challengesMarc Tischkowitz, Elisabeth Rosser
Archives of Disease in Childhood|June 30, 2017
Fifteen years of genetic testing from a London developmental clinicSunayna Best, Elisabeth Rosser, Monika Bajaj
Ophthalmic Genetics|April 5, 2018
A case of exudative vitreoretinopathy and chorioretinal coloboma associated with microcephaly in a female with contiguous Xp11.3-11.4 deletionAnne-Marie Hinds, Elisabeth Rosser, M Ashwin Reddy
Pediatric Dermatology|June 26, 2008
Cutaneous features associated with microcephalic osteodysplastic primordial dwarfism type IINaomi Webber, Edel A O'Toole, David G Paige, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 12, 2019
Improving access to genetic testing for adults with intellectual disability: A literature review and lessons from a quality improvement project in East LondonKatherine Adlington, James Smith, Jason Crabtree, et al.
European Journal of Human Genetics : EJHG|October 13, 2017
22 Years of predictive testing for Huntington's disease: the experience of the UK Huntington's Prediction ConsortiumSheharyar S Baig, Mark Strong, Elisabeth Rosser, et al.
European Journal of Human Genetics : EJHG|May 12, 2016
22 Years of predictive testing for Huntington's disease: the experience of the UK Huntington's Prediction ConsortiumSheharyar S Baig, Mark Strong, Elisabeth Rosser, et al.
European Journal of Human Genetics : EJHG|March 12, 2015
Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1Lemuel Racacho, Ashley M Byrnes, Heather MacDonald, et al.
Neurogenetics|September 14, 2006
Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelinationNicole I Wolf, Maria Cundall, Paul Rutland, et al.
European Journal of Human Genetics : EJHG|June 11, 2015
The use of whole-exome sequencing to disentangle complex phenotypesHywel J Williams, John R Hurst, Louise Ocaka, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
European Journal of Cancer (Oxford, England : 1990)|November 3, 2004
Inherited cancer in children: practical/ethical problems and challengesMarc Tischkowitz, Elisabeth Rosser
Archives of Disease in Childhood|June 30, 2017
Fifteen years of genetic testing from a London developmental clinicSunayna Best, Elisabeth Rosser, Monika Bajaj
Ophthalmic Genetics|April 5, 2018
A case of exudative vitreoretinopathy and chorioretinal coloboma associated with microcephaly in a female with contiguous Xp11.3-11.4 deletionAnne-Marie Hinds, Elisabeth Rosser, M Ashwin Reddy
Pediatric Dermatology|June 26, 2008
Cutaneous features associated with microcephalic osteodysplastic primordial dwarfism type IINaomi Webber, Edel A O'Toole, David G Paige, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 12, 2019
Improving access to genetic testing for adults with intellectual disability: A literature review and lessons from a quality improvement project in East LondonKatherine Adlington, James Smith, Jason Crabtree, et al.
European Journal of Human Genetics : EJHG|October 13, 2017
22 Years of predictive testing for Huntington's disease: the experience of the UK Huntington's Prediction ConsortiumSheharyar S Baig, Mark Strong, Elisabeth Rosser, et al.
European Journal of Human Genetics : EJHG|May 12, 2016
22 Years of predictive testing for Huntington's disease: the experience of the UK Huntington's Prediction ConsortiumSheharyar S Baig, Mark Strong, Elisabeth Rosser, et al.
European Journal of Human Genetics : EJHG|March 12, 2015
Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1Lemuel Racacho, Ashley M Byrnes, Heather MacDonald, et al.
Neurogenetics|September 14, 2006
Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelinationNicole I Wolf, Maria Cundall, Paul Rutland, et al.
European Journal of Human Genetics : EJHG|June 11, 2015
The use of whole-exome sequencing to disentangle complex phenotypesHywel J Williams, John R Hurst, Louise Ocaka, et al.
Pageof 3