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E Haan

Showing results (1-10 of 61) with videos related to

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Clinical Dysmorphology|April 18, 1998
Autosomal dominant Klippel-Feil anomaly with cleft palateE Thompson, E Haan, L Sheffield
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.
American Journal of Medical Genetics|August 22, 2000
Acampomelic campomelic dysplasia with SOX9 mutationM K Thong, G Scherer, K Kozlowski, et al.
Archives of Disease in Childhood|August 21, 2007
Fetal alcohol syndrome: a prospective national surveillance studyE J Elliott, J Payne, A Morris, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|March 6, 2003
A novel method to obtain protein release from porous polymer scaffolds: emulsion coatingJ Sohier, R E Haan, K de Groot, et al.
Journal of Medical Genetics|May 1, 1997
Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomyA Smith, R Marks, E Haan, et al.
Paediatric and Perinatal Epidemiology|October 1, 1993
Amniotic band syndrome: a population-based study in two Australian statesC Bower, F Norwood, S Knowles, et al.
Prenatal Diagnosis|April 1, 1997
First-trimester diagnosis of Smith-Lemli-Opitz syndromeP Sharp, E Haan, J M Fletcher, et al.
Pageof 7

Showing results (1-10 of 61) with videos related to

Sort By:
Pageof 7
Clinical Dysmorphology|April 18, 1998
Autosomal dominant Klippel-Feil anomaly with cleft palateE Thompson, E Haan, L Sheffield
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.
American Journal of Medical Genetics|August 22, 2000
Acampomelic campomelic dysplasia with SOX9 mutationM K Thong, G Scherer, K Kozlowski, et al.
Archives of Disease in Childhood|August 21, 2007
Fetal alcohol syndrome: a prospective national surveillance studyE J Elliott, J Payne, A Morris, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|March 6, 2003
A novel method to obtain protein release from porous polymer scaffolds: emulsion coatingJ Sohier, R E Haan, K de Groot, et al.
Journal of Medical Genetics|May 1, 1997
Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomyA Smith, R Marks, E Haan, et al.
Paediatric and Perinatal Epidemiology|October 1, 1993
Amniotic band syndrome: a population-based study in two Australian statesC Bower, F Norwood, S Knowles, et al.
Prenatal Diagnosis|April 1, 1997
First-trimester diagnosis of Smith-Lemli-Opitz syndromeP Sharp, E Haan, J M Fletcher, et al.
Pageof 7