Citrullinaemia: The possibility of prenatal diagnosis

Author:

Christensen E.,Brandt N. J.,Philip J.,Kennaway N. G.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. Christensen, E. and Brandt, N. J. Studies on glutaryl-CoA dehydrogenase in leucocytes, fibroblasts and amniotic fluid cells. The normal enzyme and the mutant form in patients with glutaric aciduria.Clin. Chim. Acta 88 (1978) 267–276

2. Christensen, E. and Hertel, J. Diagnosis and control of treatment of inborn errors of the amino acid metabolism: advantages and disadvantages of the use of an automatic amino acid analyzer with fluorescence detection. In:Amino Acid Analysis in Clinical Chemistry and Medical Research. Ellis Horwood Ltd, Chichester, England (in press)

3. Kennaway, N. G., Harwood, P. J., Ramberg, D. A., Koler, R. D. and Buist, N. R. M. Citrullinemia: enzymatic evidence for genetic heterogeneity.Pediatr. Res. 9 (1975) 554–558

4. Lockridge, O., Spector, E. and Bloom, A. D. Argininosuccinate synthetase activity in cultured human lymphocytes.Biochem. Genet. 15 (1977) 395–407

5. Mohandas, T., Miles, J., Sparkes, R. C., Sparkes, M. C., Passage, M. B. and Kaback, M. M. Assignment adenosine deaminase (ADA) to the long arm of chromosome 20: cytogenetic and somatic cell studies in an X/20 translocation.Am. J. Hum. Genet. 30 (1978) 133A

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