Proportions of spontaneous mutations in males and females with ornithine transcarbamylase deficiency
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference23 articles.
1. (1989): Urea cycle enzymes. In (eds): “The Metabolic Basis of Inherited Disease.” New York: McGraw-Hill, pp 629-663.
2. Restriction sites containing CpG show a higher frequency of polymorphism in human DNA
3. A probable sex difference in mutation rates in ornithine transcarbamylase deficiency
4. Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis.
5. Sporadic occurrence of Duchenne Muscular Dystrophy: evidence for new mutation
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