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I C Lyon

Showing results (11-20 of 19) with videos related to

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Archives of Disease in Childhood|June 1, 1976
Letter: Maternal histidinaemiaI C Lyon, R J Gardner, A M Veale
The New Zealand Medical Journal|July 1, 1972
Neonatal blood tyrosine elevationsA 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 fibrosisI C Lyon, J R Crossley, P A Smith
Archives of Disease in Childhood|July 1, 1974
Maternal histidinaemiaI C Lyon, R J Gardner, A M Veale
Humangenetik|May 26, 1975
Galactosaemia: estimated live birth incidence in New ZealandI C Lyon, C J Chapman, I B Houston, et al.
The New England Journal of Medicine|May 29, 1986
Screening for biotinidase deficiencyI C Lyon, E A Mitchell, E K Atherton, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Transient neonatal tyrosinaemiaD 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 deficiencyS Y Pang, M A Wallace, L Hofman, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 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 histidinaemiaI C Lyon, R J Gardner, A M Veale
The New Zealand Medical Journal|July 1, 1972
Neonatal blood tyrosine elevationsA 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 fibrosisI C Lyon, J R Crossley, P A Smith
Archives of Disease in Childhood|July 1, 1974
Maternal histidinaemiaI C Lyon, R J Gardner, A M Veale
Humangenetik|May 26, 1975
Galactosaemia: estimated live birth incidence in New ZealandI C Lyon, C J Chapman, I B Houston, et al.
The New England Journal of Medicine|May 29, 1986
Screening for biotinidase deficiencyI C Lyon, E A Mitchell, E K Atherton, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Transient neonatal tyrosinaemiaD 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 deficiencyS Y Pang, M A Wallace, L Hofman, et al.
Pageof 2