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E Haan

Showing results (1-10 of 71) with videos related to

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Notes and Queries|June 1, 1997
Milton and two Italian humanists: some hitherto unnoticed neo-Latin echoes in In obitum procancellarii medici and In obitum praesulis eliensisE Haan
Clinical Dysmorphology|May 8, 1998
SHORT syndrome: distinctive radiographic featuresE Haan, L Morris
The Medical Journal of Australia|February 6, 1989
Consanguinity and birth defectsA F Connon, E Haan
American Journal of Medical Genetics|September 1, 1986
Familial occurrence of Brachmann-de Lange syndromeA Bankier, E Haan, R Birrell
Clinical Dysmorphology|April 18, 1998
Autosomal dominant Klippel-Feil anomaly with cleft palateE Thompson, E Haan, L Sheffield
American Journal of Medical Genetics|July 12, 1996
Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470)A Gedeon, J Mulley, E Haan
Human Mutation|April 24, 1999
A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy. Mutation in brief no. 125. OnlineA Donnelly, E Haan, J Manson, et al.
Australian Dental Journal|October 1, 1994
Familial hemifacial microsomia due to autosomal dominant inheritance. Case reportsS L Singer, E Haan, J Slee, et al.
Clinical Genetics|January 24, 1998
Osteopathia striata with cranial sclerosis: highly variable phenotypic expression within a familyR Savarirayan, J Nance, L Morris, et al.
The Medical Journal of Australia|January 20, 1986
Leigh's diseaseJ McGill, T Maddison, K Collins, et al.
Pageof 8

Showing results (1-10 of 71) with videos related to

Sort By:
Pageof 8
Notes and Queries|June 1, 1997
Milton and two Italian humanists: some hitherto unnoticed neo-Latin echoes in In obitum procancellarii medici and In obitum praesulis eliensisE Haan
Clinical Dysmorphology|May 8, 1998
SHORT syndrome: distinctive radiographic featuresE Haan, L Morris
The Medical Journal of Australia|February 6, 1989
Consanguinity and birth defectsA F Connon, E Haan
American Journal of Medical Genetics|September 1, 1986
Familial occurrence of Brachmann-de Lange syndromeA Bankier, E Haan, R Birrell
Clinical Dysmorphology|April 18, 1998
Autosomal dominant Klippel-Feil anomaly with cleft palateE Thompson, E Haan, L Sheffield
American Journal of Medical Genetics|July 12, 1996
Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470)A Gedeon, J Mulley, E Haan
Human Mutation|April 24, 1999
A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy. Mutation in brief no. 125. OnlineA Donnelly, E Haan, J Manson, et al.
Australian Dental Journal|October 1, 1994
Familial hemifacial microsomia due to autosomal dominant inheritance. Case reportsS L Singer, E Haan, J Slee, et al.
Clinical Genetics|January 24, 1998
Osteopathia striata with cranial sclerosis: highly variable phenotypic expression within a familyR Savarirayan, J Nance, L Morris, et al.
The Medical Journal of Australia|January 20, 1986
Leigh's diseaseJ McGill, T Maddison, K Collins, et al.
Pageof 8