R B Gordon|J W Rutledge - JoVE Visualize

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The Journal of Nutrition|April 1, 1996

Human homocysteine catabolism: three major pathways and their relevance to development of arterial occlusive diseaseN P Dudman, X W Guo, R B Gordon, et al.

Journal of Inherited Metabolic Disease|January 1, 1990

Identification of a single nucleotide substitution in the coding sequence of in vitro amplified cDNA from a patient with partial HPRT deficiency (HPRTBRISBANE)R B Gordon, D G Sculley, P A Dawson, et al.

Australian and New Zealand Journal of Medicine|December 1, 1984

Renal failure in infancy due to over-production of urateJ A Batch, R P Riek, R B Gordon, et al.

Human Genetics|October 1, 1991

Hypoxanthine-guanine phosphoribosyltransferase deficiency: analysis of HPRT mutations by direct sequencing and allele-specific amplificationD G Sculley, P A Dawson, I R Beacham, et al.

AJR. American Journal of Roentgenology|October 1, 1986

CT of appendicitisE J Balthazar, A J Megibow, D Hulnick, et al.

Radiology|September 1, 1987

Perforated colorectal neoplasms: correlation of clinical, contrast enema, and CT examinationsD H Hulnick, A J Megibow, E J Balthazar, et al.

Biochimica Et Biophysica Acta|October 23, 1990

Expression of active human hypoxanthine-guanine phosphoribosyltransferase in Escherichia coli and characterisation of the recombinant enzymeM L Free, R B Gordon, D T Keough, et al.

Human Mutation|April 24, 1999

Mutational analysis of the cystathionine beta-synthase gene: a splicing mutation, two missense mutations and an insertion in patients with homocystinuria. Mutations in brief no. 120. OnlineR B Gordon, A J Cox, P A Dawson, et al.

European Journal of Human Genetics : EJHG|January 1, 1997

Characterisation of five missense mutations in the cystathionine beta-synthase gene from three patients with B6-nonresponsive homocystinuriaP A Dawson, A J Cox, B T Emmerson, et al.

Gene|December 15, 1991

The molecular characterisation of HPRT CHERMSIDE and HPRT COORPAROO: two Lesch-Nyhan patients with reduced amounts of mRNAR B Gordon, P A Dawson, D G Sculley, et al.

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Showing results (31-40 of 47) with videos related to

Sort By:

Pageof 5

The Journal of Nutrition|April 1, 1996

Human homocysteine catabolism: three major pathways and their relevance to development of arterial occlusive diseaseN P Dudman, X W Guo, R B Gordon, et al.

Journal of Inherited Metabolic Disease|January 1, 1990

Identification of a single nucleotide substitution in the coding sequence of in vitro amplified cDNA from a patient with partial HPRT deficiency (HPRTBRISBANE)R B Gordon, D G Sculley, P A Dawson, et al.

Australian and New Zealand Journal of Medicine|December 1, 1984

Renal failure in infancy due to over-production of urateJ A Batch, R P Riek, R B Gordon, et al.

Human Genetics|October 1, 1991

Hypoxanthine-guanine phosphoribosyltransferase deficiency: analysis of HPRT mutations by direct sequencing and allele-specific amplificationD G Sculley, P A Dawson, I R Beacham, et al.

AJR. American Journal of Roentgenology|October 1, 1986

CT of appendicitisE J Balthazar, A J Megibow, D Hulnick, et al.

Radiology|September 1, 1987

Perforated colorectal neoplasms: correlation of clinical, contrast enema, and CT examinationsD H Hulnick, A J Megibow, E J Balthazar, et al.

Biochimica Et Biophysica Acta|October 23, 1990

Expression of active human hypoxanthine-guanine phosphoribosyltransferase in Escherichia coli and characterisation of the recombinant enzymeM L Free, R B Gordon, D T Keough, et al.

Human Mutation|April 24, 1999

Mutational analysis of the cystathionine beta-synthase gene: a splicing mutation, two missense mutations and an insertion in patients with homocystinuria. Mutations in brief no. 120. OnlineR B Gordon, A J Cox, P A Dawson, et al.

European Journal of Human Genetics : EJHG|January 1, 1997

Characterisation of five missense mutations in the cystathionine beta-synthase gene from three patients with B6-nonresponsive homocystinuriaP A Dawson, A J Cox, B T Emmerson, et al.

Gene|December 15, 1991

The molecular characterisation of HPRT CHERMSIDE and HPRT COORPAROO: two Lesch-Nyhan patients with reduced amounts of mRNAR B Gordon, P A Dawson, D G Sculley, et al.

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