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

A gene specific DNA probe has been used to predict the genotype of two fetuses in families at risk for ornithine carbamoyl transferase deficiency. Although the probe does not detect the mutation directly, prediction was possible by examining restriction fragment length polymorphisms of the parents a...

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Bibliografske podrobnosti
Main Authors: Pembrey, M E, Old, J M, Leonard, J V, Rodeck, C H, Warren, R, Davies, K E
Format: Artigo
Jezik:Inglês
Izdano: 1985
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049507/
https://ncbi.nlm.nih.gov/pubmed/3001312
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