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D T Whelan

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Biochemical Medicine|January 1, 1974
Microassay of tyrosine-amino transferase and p-hydroxyphenylpyruvic acid oxidase in mammalian liver and patients with hereditary tyrosinemiaD T Whelan, V G Zannoni
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 13, 1984
Mass spectrometry and clinical chemistryR E Hill, D T Whelan
Lancet (London, England)|November 1, 1980
Maternal hyperprolinaemiaD T Whelan, W T Conner
Clinical Genetics|April 1, 1980
A rare case of mosaic Down syndrome 46,XY/46,XY, -21, +i(21q)I A Uchida, D T Whelan
Clinical Genetics|September 1, 1975
The oro-facial-digital syndromeD T Whelan, W Feldman, I Dost
Pediatrics|June 1, 1976
Citrullinemia: phenotypic variationsD T Whelan, T Brusso, M Spate
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1983
Fumaric aciduria: a new organic aciduria, associated with mental retardation and speech impairmentD T Whelan, R E Hill, S McClorry
American Journal of Medical Genetics|August 26, 1998
Smith-Lemli-Opitz syndrome: phenotypic extreme with minimal clinical findingsM J Nowaczyk, D T Whelan, R E Hill
Teratology|October 1, 1987
Experimental hyperphenylalaninemia in the pregnant guinea pig: possible phenylalanine teratogenesis and p-chlorophenylalanine embryotoxicityJ B Kronick, D T Whelan, D J McCallion
Clinical Genetics|August 1, 1983
Mucolipidosis II. The clinical, radiological and biochemical features in three casesD T Whelan, P L Chang, P W Cockshott
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Biochemical Medicine|January 1, 1974
Microassay of tyrosine-amino transferase and p-hydroxyphenylpyruvic acid oxidase in mammalian liver and patients with hereditary tyrosinemiaD T Whelan, V G Zannoni
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 13, 1984
Mass spectrometry and clinical chemistryR E Hill, D T Whelan
Lancet (London, England)|November 1, 1980
Maternal hyperprolinaemiaD T Whelan, W T Conner
Clinical Genetics|April 1, 1980
A rare case of mosaic Down syndrome 46,XY/46,XY, -21, +i(21q)I A Uchida, D T Whelan
Clinical Genetics|September 1, 1975
The oro-facial-digital syndromeD T Whelan, W Feldman, I Dost
Pediatrics|June 1, 1976
Citrullinemia: phenotypic variationsD T Whelan, T Brusso, M Spate
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1983
Fumaric aciduria: a new organic aciduria, associated with mental retardation and speech impairmentD T Whelan, R E Hill, S McClorry
American Journal of Medical Genetics|August 26, 1998
Smith-Lemli-Opitz syndrome: phenotypic extreme with minimal clinical findingsM J Nowaczyk, D T Whelan, R E Hill
Teratology|October 1, 1987
Experimental hyperphenylalaninemia in the pregnant guinea pig: possible phenylalanine teratogenesis and p-chlorophenylalanine embryotoxicityJ B Kronick, D T Whelan, D J McCallion
Clinical Genetics|August 1, 1983
Mucolipidosis II. The clinical, radiological and biochemical features in three casesD T Whelan, P L Chang, P W Cockshott
Pageof 3