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Items: 9

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Family studies in ornithine transcarbamylase deficiency.

Svirklys LG, Wilcken B, Hammond J, Mackinlay AG, O'Sullivan WJ.

Arch Dis Child. 1988 Mar;63(3):297-302.

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Prenatal diagnosis of common genetic disorders.

Crawfurd MD.

BMJ. 1988 Aug 20-27;297(6647):502-6. Review. No abstract available.

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New mutation and prenatal diagnosis in ornithine transcarbamylase deficiency.

Nussbaum RL, Boggs BA, Beaudet AL, Doyle S, Potter JL, O'Brien WE.

Am J Hum Genet. 1986 Feb;38(2):149-58.

8.

Prenatal diagnosis of ornithine carbamoyl transferase deficiency using a gene specific probe.

Pembrey ME, Old JM, Leonard JV, Rodeck CH, Warren R, Davies KE.

J Med Genet. 1985 Dec;22(6):462-5.

9.

Prenatal diagnosis of enzyme defects.

Winchester B.

Arch Dis Child. 1990 Jan;65(1 Spec No):59-67. Review. No abstract available.

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