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E Haan

Showing results (11-20 of 71) with videos related to

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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.
Paediatric and Perinatal Epidemiology|June 10, 1998
A population-based study of abdominal wall defects in South Australia and Western AustraliaR Byron-Scott, E Haan, A Chan, et al.
Human Mutation|February 6, 1998
A type III collagen Gly559 to Arg helix mutation in Ehler's-Danlos syndrome type IVJ F Bateman, A A Chiodo, Y M Weng, et al.
Clinical Genetics|July 16, 2003
X-linked myotubular myopathy in a family with three adult survivorsS Yu, J Manson, S White, et al.
Archives of Disease in Childhood|February 25, 2003
Birth prevalence of Prader-Willi syndrome in AustraliaA Smith, J Egan, G Ridley, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
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.
Paediatric and Perinatal Epidemiology|June 10, 1998
A population-based study of abdominal wall defects in South Australia and Western AustraliaR Byron-Scott, E Haan, A Chan, et al.
Human Mutation|February 6, 1998
A type III collagen Gly559 to Arg helix mutation in Ehler's-Danlos syndrome type IVJ F Bateman, A A Chiodo, Y M Weng, et al.
Clinical Genetics|July 16, 2003
X-linked myotubular myopathy in a family with three adult survivorsS Yu, J Manson, S White, et al.
Archives of Disease in Childhood|February 25, 2003
Birth prevalence of Prader-Willi syndrome in AustraliaA Smith, J Egan, G Ridley, et al.
Pageof 8