Molecular analysis of the inheritance of phenylketonuria and mild hyperphenylalaninemia in families with both disorders.

No abstract is available for this paper.

• Publication year

  1986

• Venue

  New England Journal of Medicine

• Publication date

  1986-05-15

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1056/NEJM198605153142002PMID 3702929
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  1986cited by this paper
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  1985cited by this paper
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  1985cited by this paper
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  1985cited by this paper
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  1985cited by this paper
• Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria.

  1985cited by this paper
• Compound heterozygotes in hyperphenylalaninaemia.

  1984cited by this paper
• Prenatal diagnosis of classical phenylketonuria by gene mapping.

  1984cited by this paper
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  1982cited by this paper
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  1980cited by this paper
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  1980cited by this paper
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  1980cited by this paper
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  1980cited by this paper
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  1977cited by this paper
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  1977cited by this paper
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  1975cited by this paper
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  1973cited by this paper
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  1973cited by this paper
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  1971cited by this paper
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  1969cited by this paper
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  1969cited by this paper
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  1968cited by this paper
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  1997cites this paper
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• Erratum

  1994cites this paper
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  1994cites this paper
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  1994cites this paper
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  1991cites this paper
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  1991influential citation
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  1991cites this paper
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