Search research articles
Contact Us
Filters
Showing results (11-20 of 19) with videos related to
Page
of 2
Sort By:
You have reached the last page of results.
This site can display upto 19 results.
Archives of Disease in Childhood
|
June 1, 1976
Letter: Maternal histidinaemia
I C Lyon, R J Gardner, A M Veale
The New Zealand Medical Journal
|
July 1, 1972
Neonatal blood tyrosine elevations
A M Veale, I C Lyon, I B Houston
Journal of Inherited Metabolic Disease
|
January 1, 1985
Outcome of pregnancy in the rat with mild hyperphenylalaninaemia and hypertyrosinaemia: implications for the management of "human maternal PKU"
S A Lewis, I C Lyon, R B Elliott
The New Zealand Medical Journal
|
September 14, 1983
Screening for cystic fibrosis
I C Lyon, J R Crossley, P A Smith
Archives of Disease in Childhood
|
July 1, 1974
Maternal histidinaemia
I C Lyon, R J Gardner, A M Veale
Humangenetik
|
May 26, 1975
Galactosaemia: estimated live birth incidence in New Zealand
I C Lyon, C J Chapman, I B Houston, et al.
The New England Journal of Medicine
|
May 29, 1986
Screening for biotinidase deficiency
I C Lyon, E A Mitchell, E K Atherton, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Transient neonatal tyrosinaemia
D N Rice, I B Houston, I C Lyon, et al.
Pediatrics
|
June 1, 1988
Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
S Y Pang, M A Wallace, L Hofman, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Archives of Disease in Childhood
|
June 1, 1976
Letter: Maternal histidinaemia
I C Lyon, R J Gardner, A M Veale
The New Zealand Medical Journal
|
July 1, 1972
Neonatal blood tyrosine elevations
A M Veale, I C Lyon, I B Houston
Journal of Inherited Metabolic Disease
|
January 1, 1985
Outcome of pregnancy in the rat with mild hyperphenylalaninaemia and hypertyrosinaemia: implications for the management of "human maternal PKU"
S A Lewis, I C Lyon, R B Elliott
The New Zealand Medical Journal
|
September 14, 1983
Screening for cystic fibrosis
I C Lyon, J R Crossley, P A Smith
Archives of Disease in Childhood
|
July 1, 1974
Maternal histidinaemia
I C Lyon, R J Gardner, A M Veale
Humangenetik
|
May 26, 1975
Galactosaemia: estimated live birth incidence in New Zealand
I C Lyon, C J Chapman, I B Houston, et al.
The New England Journal of Medicine
|
May 29, 1986
Screening for biotinidase deficiency
I C Lyon, E A Mitchell, E K Atherton, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Transient neonatal tyrosinaemia
D N Rice, I B Houston, I C Lyon, et al.
Pediatrics
|
June 1, 1988
Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
S Y Pang, M A Wallace, L Hofman, et al.
Page
of 2