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Journal of Paediatrics and Child Health
|
September 4, 1998
Prader-Willi syndrome: a new study of the Australian Paediatric Surveillance Unit
A 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 gene
M 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 gut
E 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 dilemma
M 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 syndrome
A 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 acidemia
R 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 spectrometry
A 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 Australia
A 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 localization
A Harris, S Lankester, E Haan, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 71) with videos related to
Sort By:
Page
of 8
Journal of Paediatrics and Child Health
|
September 4, 1998
Prader-Willi syndrome: a new study of the Australian Paediatric Surveillance Unit
A 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 gene
M 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 gut
E 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 dilemma
M 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 syndrome
A 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 acidemia
R 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 spectrometry
A 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 Australia
A 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 localization
A Harris, S Lankester, E Haan, et al.
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of 8