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E Haan

Showing results (21-30 of 71) with videos related to

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Journal of Paediatrics and Child Health|September 4, 1998
Prader-Willi syndrome: a new study of the Australian Paediatric Surveillance UnitA Smith, E Haan, G Warne, et al.
Developmental Medicine and Child Neurology|September 24, 1998
What constitutes cerebral palsy?N Badawi, L Watson, B Petterson, et al.
European Journal of Biochemistry|September 24, 1998
Preferential pre-mRNA utilisation of an upstream cryptic 5' splice site created by a single base deletion mutation in exon 37 of the FBN-1 geneM A Gibson, S L Ellis, L C Ades, et al.
European Journal of Pediatrics|May 1, 1985
Severe illness caused by the products of bacterial metabolism in a child with a short gutE Haan, G Brown, A Bankier, et al.
Clinical Dysmorphology|October 26, 1999
A child with hemimegalencephaly, hemihypertrophy, macrocephaly, cutaneous vascular malformation, psychomotor retardation and intestinal lymphangiectasia--a diagnostic dilemmaM K Thong, E Thompson, R Keenan, et al.
Human Genetics|March 1, 1991
A de novo unbalanced reciprocal translocation identified as paternal in origin in the Prader-Willi syndromeA Smith, R Lindeman, F Volpato, et al.
Biomedical Mass Spectrometry|July 1, 1979
The identification of 3-keto-2-methylvaleric acid and 3-hydroxy-2-methylvaleric acid in a patient with propionic acidemiaR J Truscott, C J Pullin, B Halpern, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 15, 1988
A new method for the determination of L-dopa and 3-O-methyldopa in plasma and cerebrospinal fluid using gas chromatography and electron capture negative ion mass spectrometryA P de Jong, R M Kok, C A Cramers, et al.
The Medical Journal of Australia|August 2, 2001
"Folate before pregnancy": the impact on women and health professionals of a population-based health promotion campaign in South AustraliaA Chan, J Pickering, E Haan, et al.
Clinical Genetics|July 1, 1988
The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localizationA Harris, S Lankester, E Haan, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
Journal of Paediatrics and Child Health|September 4, 1998
Prader-Willi syndrome: a new study of the Australian Paediatric Surveillance UnitA Smith, E Haan, G Warne, et al.
Developmental Medicine and Child Neurology|September 24, 1998
What constitutes cerebral palsy?N Badawi, L Watson, B Petterson, et al.
European Journal of Biochemistry|September 24, 1998
Preferential pre-mRNA utilisation of an upstream cryptic 5' splice site created by a single base deletion mutation in exon 37 of the FBN-1 geneM A Gibson, S L Ellis, L C Ades, et al.
European Journal of Pediatrics|May 1, 1985
Severe illness caused by the products of bacterial metabolism in a child with a short gutE Haan, G Brown, A Bankier, et al.
Clinical Dysmorphology|October 26, 1999
A child with hemimegalencephaly, hemihypertrophy, macrocephaly, cutaneous vascular malformation, psychomotor retardation and intestinal lymphangiectasia--a diagnostic dilemmaM K Thong, E Thompson, R Keenan, et al.
Human Genetics|March 1, 1991
A de novo unbalanced reciprocal translocation identified as paternal in origin in the Prader-Willi syndromeA Smith, R Lindeman, F Volpato, et al.
Biomedical Mass Spectrometry|July 1, 1979
The identification of 3-keto-2-methylvaleric acid and 3-hydroxy-2-methylvaleric acid in a patient with propionic acidemiaR J Truscott, C J Pullin, B Halpern, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 15, 1988
A new method for the determination of L-dopa and 3-O-methyldopa in plasma and cerebrospinal fluid using gas chromatography and electron capture negative ion mass spectrometryA P de Jong, R M Kok, C A Cramers, et al.
The Medical Journal of Australia|August 2, 2001
"Folate before pregnancy": the impact on women and health professionals of a population-based health promotion campaign in South AustraliaA Chan, J Pickering, E Haan, et al.
Clinical Genetics|July 1, 1988
The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localizationA Harris, S Lankester, E Haan, et al.
Pageof 8