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Links from PubMed

Items: 7

1.

Citrullinaemia with rapidly fatal neonatal course.

Van Der Zee SP, Trijbels JM, Monnens LA, Hommes FA, Schretlen ED.

Arch Dis Child. 1971 Dec;46(250):847-51. No abstract available.

2.

The human argininosuccinate synthetase locus and citrullinemia.

Beaudet AL, O'Brien WE, Bock HG, Freytag SO, Su TS.

Adv Hum Genet. 1986;15:161-96, 291-2. Review. No abstract available.

PMID:
3513483
3.

Metabolic errors in lysine degradation.

Carson NA.

Clin Endocrinol Metab. 1974 Mar;3(1):71-86. Review. No abstract available.

PMID:
4609650
4.

[Enzymatic analysis of citrullinemia in Japan].

Saheki T.

Seikagaku. 1982;54(7):435-43. Review. Japanese. No abstract available.

PMID:
6754830
5.

Diagnosis and mangement of inherited aminoacidopathies in the newborn and the unborn.

Rosenberg LE.

Clin Endocrinol Metab. 1974 Mar;3(1):145-52. Review. No abstract available.

PMID:
4609645
6.

Screening for inborn errors of amino acid metabolism.

Wu JT.

Ann Clin Lab Sci. 1991 Mar-Apr;21(2):123-42. Review.

PMID:
2029175
7.

Molecular basis of hereditary disease.

Harris H.

Br Med J. 1968 Apr 20;2(5598):135-41. Review. No abstract available.

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