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N S Van De Water

Showing results (1-10 of 28) with videos related to

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The New Zealand Medical Journal|September 14, 1988
Haemophilia carrier detection using DNA analysisN S Van-de-Water, P A Ockelford
Journal of Medical Genetics|March 1, 1991
Restriction fragment length polymorphisms associated with the factor VIII and factor IX genes in PolynesiansN S Van-de-Water, D Ridgway, P A Ockelford
Biochemical Medicine|December 1, 1977
Heterozygote detection: a comparative study using neutrophils, lymphocytes, and two reference parameters in the bovine mannosidosis modelR D Jolly, A Janmaat, N S van de Water
The Australian Journal of Experimental Biology and Medical Science|October 1, 1979
Canine Gaucher disease--the enzymic defectN S Van De Water, R D Jolly, B R Farrow
The Biochemical Journal|July 1, 1976
The nature of the residual alpha-mannosidase in plasma in bovine mannosidosisB G Winchester, N S Van-de-Water, R D Jolly
The New Zealand Medical Journal|February 8, 1989
DNA diagnosis in haemophilia management: who will pay to save?N S Van-de-Water, P A Ockelford, E W Berry
British Journal of Haematology|November 1, 1994
Possible misdiagnosis using the Xba I polymorphism for prenatal diagnosis of haemophilia AN S Van de Water, S J May, P J Browett
Pathology|January 1, 1995
Factor VIII gene inversions in severe hemophilia A patientsN S Van de Water, R Williams, J Nelson, et al.
Gut|March 1, 1995
Analysis of Ha-ras 1 allele frequencies in hereditary non-polyposis colorectal cancerP Jeevaratnam, P J Browett, N S Van de Water, et al.
Australian and New Zealand Journal of Medicine|June 1, 1995
A brave new world of cancer screeningJ R Jass, P J Browett, N S Van de Water, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
The New Zealand Medical Journal|September 14, 1988
Haemophilia carrier detection using DNA analysisN S Van-de-Water, P A Ockelford
Journal of Medical Genetics|March 1, 1991
Restriction fragment length polymorphisms associated with the factor VIII and factor IX genes in PolynesiansN S Van-de-Water, D Ridgway, P A Ockelford
Biochemical Medicine|December 1, 1977
Heterozygote detection: a comparative study using neutrophils, lymphocytes, and two reference parameters in the bovine mannosidosis modelR D Jolly, A Janmaat, N S van de Water
The Australian Journal of Experimental Biology and Medical Science|October 1, 1979
Canine Gaucher disease--the enzymic defectN S Van De Water, R D Jolly, B R Farrow
The Biochemical Journal|July 1, 1976
The nature of the residual alpha-mannosidase in plasma in bovine mannosidosisB G Winchester, N S Van-de-Water, R D Jolly
The New Zealand Medical Journal|February 8, 1989
DNA diagnosis in haemophilia management: who will pay to save?N S Van-de-Water, P A Ockelford, E W Berry
British Journal of Haematology|November 1, 1994
Possible misdiagnosis using the Xba I polymorphism for prenatal diagnosis of haemophilia AN S Van de Water, S J May, P J Browett
Pathology|January 1, 1995
Factor VIII gene inversions in severe hemophilia A patientsN S Van de Water, R Williams, J Nelson, et al.
Gut|March 1, 1995
Analysis of Ha-ras 1 allele frequencies in hereditary non-polyposis colorectal cancerP Jeevaratnam, P J Browett, N S Van de Water, et al.
Australian and New Zealand Journal of Medicine|June 1, 1995
A brave new world of cancer screeningJ R Jass, P J Browett, N S Van de Water, et al.
Pageof 3