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A H Child

Showing results (31-40 of 45) with videos related to

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The British Journal of Dermatology|January 29, 2000
Distichiasis-lymphoedema: clinical features, venous function and lymphoscintigraphyJ L Rosbotham, G W Brice, A H Child, et al.
Genetic Counseling (Geneva, Switzerland)|November 11, 2008
Scoliosis, blindness and arachnodactyly in a large Turkish family: is it a new syndrome?M Dundar, K Erkilic, M Argun, et al.
Journal of Medical Genetics|February 4, 2005
Milroy disease and the VEGFR-3 mutation phenotypeG Brice, A H Child, A Evans, et al.
Journal of Medical Genetics|September 10, 2003
Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedemaA L Evans, R Bell, G Brice, et al.
Journal of Medical Genetics|August 16, 2003
Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testingT Aung, N D Ebenezer, G Brice, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2003
Muscle fibrillin deficiency in Marfan's syndrome myopathyW M H Behan, C Longman, R K H Petty, et al.
The New England Journal of Medicine|April 2, 1992
Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative StudyP Tsipouras, R Del Mastro, M Sarfarazi, et al.
Journal of Medical Genetics|February 1, 1990
Linkage data for Marfan syndrome and markers on chromosomes 1 and 11J de Groote, P A Farndon, M V Kilpatrick, et al.
Journal of Medical Genetics|February 24, 2001
Reduction of the genetic interval for lyphoedema-distichiasis to below 2 MbR Bell, G Brice, A H Child, et al.
The British Journal of Ophthalmology|January 25, 2003
The phenotype of normal tension glaucoma patients with and without OPA1 polymorphismsT Aung, K Okada, D Poinoosawmy, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
The British Journal of Dermatology|January 29, 2000
Distichiasis-lymphoedema: clinical features, venous function and lymphoscintigraphyJ L Rosbotham, G W Brice, A H Child, et al.
Genetic Counseling (Geneva, Switzerland)|November 11, 2008
Scoliosis, blindness and arachnodactyly in a large Turkish family: is it a new syndrome?M Dundar, K Erkilic, M Argun, et al.
Journal of Medical Genetics|February 4, 2005
Milroy disease and the VEGFR-3 mutation phenotypeG Brice, A H Child, A Evans, et al.
Journal of Medical Genetics|September 10, 2003
Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedemaA L Evans, R Bell, G Brice, et al.
Journal of Medical Genetics|August 16, 2003
Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testingT Aung, N D Ebenezer, G Brice, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2003
Muscle fibrillin deficiency in Marfan's syndrome myopathyW M H Behan, C Longman, R K H Petty, et al.
The New England Journal of Medicine|April 2, 1992
Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative StudyP Tsipouras, R Del Mastro, M Sarfarazi, et al.
Journal of Medical Genetics|February 1, 1990
Linkage data for Marfan syndrome and markers on chromosomes 1 and 11J de Groote, P A Farndon, M V Kilpatrick, et al.
Journal of Medical Genetics|February 24, 2001
Reduction of the genetic interval for lyphoedema-distichiasis to below 2 MbR Bell, G Brice, A H Child, et al.
The British Journal of Ophthalmology|January 25, 2003
The phenotype of normal tension glaucoma patients with and without OPA1 polymorphismsT Aung, K Okada, D Poinoosawmy, et al.
Pageof 5