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E A Haan

Showing results (11-20 of 96) with videos related to

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Archives of Disease in Childhood. Fetal and Neonatal Edition|November 1, 1994
Umbilical cord ulceration in association with intestinal atresia in a child with deletion 13q and Hirschsprung's diseaseT Y Khong, W D Ford, E A Haan
Journal of Medical Genetics|February 1, 1993
Hydrocephalus in Hajdu-Cheney syndromeL C Adès, L L Morris, E A Haan
Journal of Inherited Metabolic Disease|January 1, 1982
Carrier detection in ornithine transcarbamylase deficiencyE A Haan, D M Danks, A Grimes, et al.
BMJ (Clinical Research Ed.)|October 3, 1998
Effect of parity, gravidity, previous miscarriage, and age on risk of Down's syndrome: population based studyA Chan, K A McCaul, R J Keane, et al.
Human Genetics|February 25, 2009
The genomic basis of cerebral palsy: a HuGE systematic literature reviewM E O'Callaghan, A H MacLennan, E A Haan, et al.
American Journal of Human Genetics|November 1, 1991
Epidemiology of Down syndrome in South Australia, 1960-89A J Staples, G R Sutherland, E A Haan, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Succinic semialdehyde dehydrogenase deficiency--a further caseE A Haan, G K Brown, D Mitchell, et al.
American Journal of Medical Genetics|April 1, 1992
Use of linkage data obtained in single families: prenatal diagnosis of a new X-linked mental retardation syndromeJ C Mulley, A K Gedeon, S Wilson, et al.
American Journal of Medical Genetics|May 15, 1994
Neurological involvement in Worth type endosteal hyperostosis: report of a familyL C Adès, L L Morris, R Burns, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
A carbamylphosphate synthetase deficiency with no detectable immunoreactive enzyme and no translatable mRNAL Graf, P McIntyre, N Hoogenraad, et al.
Pageof 10

Showing results (11-20 of 96) with videos related to

Sort By:
Pageof 10
Archives of Disease in Childhood. Fetal and Neonatal Edition|November 1, 1994
Umbilical cord ulceration in association with intestinal atresia in a child with deletion 13q and Hirschsprung's diseaseT Y Khong, W D Ford, E A Haan
Journal of Medical Genetics|February 1, 1993
Hydrocephalus in Hajdu-Cheney syndromeL C Adès, L L Morris, E A Haan
Journal of Inherited Metabolic Disease|January 1, 1982
Carrier detection in ornithine transcarbamylase deficiencyE A Haan, D M Danks, A Grimes, et al.
BMJ (Clinical Research Ed.)|October 3, 1998
Effect of parity, gravidity, previous miscarriage, and age on risk of Down's syndrome: population based studyA Chan, K A McCaul, R J Keane, et al.
Human Genetics|February 25, 2009
The genomic basis of cerebral palsy: a HuGE systematic literature reviewM E O'Callaghan, A H MacLennan, E A Haan, et al.
American Journal of Human Genetics|November 1, 1991
Epidemiology of Down syndrome in South Australia, 1960-89A J Staples, G R Sutherland, E A Haan, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Succinic semialdehyde dehydrogenase deficiency--a further caseE A Haan, G K Brown, D Mitchell, et al.
American Journal of Medical Genetics|April 1, 1992
Use of linkage data obtained in single families: prenatal diagnosis of a new X-linked mental retardation syndromeJ C Mulley, A K Gedeon, S Wilson, et al.
American Journal of Medical Genetics|May 15, 1994
Neurological involvement in Worth type endosteal hyperostosis: report of a familyL C Adès, L L Morris, R Burns, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
A carbamylphosphate synthetase deficiency with no detectable immunoreactive enzyme and no translatable mRNAL Graf, P McIntyre, N Hoogenraad, et al.
Pageof 10