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Human Genetics
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January 1, 1985
Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: plasma changes and skin fibroblast phytanic acid oxidase
A Poulos, P Sharp, A J Fellenberg, et al.
American Journal of Human Genetics
|
September 1, 1983
Mutations at more than one locus may be involved in cystic fibrosis--evidence based on first-cousin data and direct counting of cases
D M Danks, J Allan, P D Phelan, et al.
BMJ (Clinical Research Ed.)
|
August 11, 1990
Wilson's disease in adults with cirrhosis but no neurological abnormalities
D M Danks, G Metz, R Sewell, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazole
E Treacy, D Johnson, J J Pitt, et al.
Journal of Medical Genetics
|
February 1, 1986
X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia
J Halliday, C W Chow, D Wallace, et al.
Lancet (London, England)
|
November 13, 1971
Is Menkes' syndrome a heritable disorder of connective tissue?
D M Danks, E Cartwright, P E Campbell, et al.
The Journal of Nutrition
|
June 1, 1991
Hepatic ceruloplasmin gene expression is unaltered in the toxic milk mouse
J F Mercer, A Grimes, D M Danks, et al.
The Biochemical Journal
|
April 15, 1981
Copper metabolism in mottled mouse (Mus musculus) mutants. Studies of blotchy (Moblo) mice and a comparison with brindled (Mobr) mice
J R Mann, J Camakaris, N Francis, et al.
Australian Paediatric Journal
|
December 1, 1980
The incidence and presentation of cystic fibrosis in Victoria 1955-1978
J L Allan, M Robbie, P D Phelan, et al.
The Biochemical Journal
|
February 15, 1982
Copper metabolism in mottled mouse mutants. The effect of copper therapy on lysyl oxidase activity in brindled (Mobr) mice
P M Royce, J Camakaris, J R Mann, et al.
Page
of 26
Search research articles
Search
Showing results (141-150 of 255) with videos related to
Sort By:
Page
of 26
Human Genetics
|
January 1, 1985
Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: plasma changes and skin fibroblast phytanic acid oxidase
A Poulos, P Sharp, A J Fellenberg, et al.
American Journal of Human Genetics
|
September 1, 1983
Mutations at more than one locus may be involved in cystic fibrosis--evidence based on first-cousin data and direct counting of cases
D M Danks, J Allan, P D Phelan, et al.
BMJ (Clinical Research Ed.)
|
August 11, 1990
Wilson's disease in adults with cirrhosis but no neurological abnormalities
D M Danks, G Metz, R Sewell, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazole
E Treacy, D Johnson, J J Pitt, et al.
Journal of Medical Genetics
|
February 1, 1986
X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia
J Halliday, C W Chow, D Wallace, et al.
Lancet (London, England)
|
November 13, 1971
Is Menkes' syndrome a heritable disorder of connective tissue?
D M Danks, E Cartwright, P E Campbell, et al.
The Journal of Nutrition
|
June 1, 1991
Hepatic ceruloplasmin gene expression is unaltered in the toxic milk mouse
J F Mercer, A Grimes, D M Danks, et al.
The Biochemical Journal
|
April 15, 1981
Copper metabolism in mottled mouse (Mus musculus) mutants. Studies of blotchy (Moblo) mice and a comparison with brindled (Mobr) mice
J R Mann, J Camakaris, N Francis, et al.
Australian Paediatric Journal
|
December 1, 1980
The incidence and presentation of cystic fibrosis in Victoria 1955-1978
J L Allan, M Robbie, P D Phelan, et al.
The Biochemical Journal
|
February 15, 1982
Copper metabolism in mottled mouse mutants. The effect of copper therapy on lysyl oxidase activity in brindled (Mobr) mice
P M Royce, J Camakaris, J R Mann, et al.
Page
of 26