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Items: 6

1.

Prenatal exclusion of ornithine transcarbamylase deficiency by direct gene analysis.

Old JM, Briand PL, Purvis-Smith S, Howard NJ, Wilcken B, Hammond J, Pearson P, Cathelineau L, Williamson R, Davies KE.

Lancet. 1985 Jan 12;1(8420):73-5.

PMID:
2857026
2.

Molecular detection and correction of ornithine transcarbamylase deficiency.

Grompe M, Jones SN, Caskey CT.

Trends Genet. 1990 Oct;6(10):335-9. Review.

PMID:
2281529
3.

The clinical, biochemical, and molecular spectrum of ornithine transcarbamylase deficiency.

Tuchman M.

J Lab Clin Med. 1992 Dec;120(6):836-50. Review. No abstract available.

PMID:
1453106
4.

The ornithine transcarbamylase (OTC) gene: mutations in 50 Japanese families with OTC deficiency.

Matsuda I, Tanase S.

Am J Med Genet. 1997 Sep 5;71(4):378-83. Review.

PMID:
9286441
5.

Mutations and polymorphisms in the human ornithine transcarbamylase gene.

Tuchman M.

Hum Mutat. 1993;2(3):174-8. Review.

PMID:
8364586
6.

Inherited hepatic enzyme defects as candidates for liver-directed gene therapy.

Horwich AL.

Curr Top Microbiol Immunol. 1991;168:185-200. Review. No abstract available.

PMID:
1893777

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