SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1).

No abstract is available for this paper.

• Publication year

  1994

• Venue

  Human Molecular Genetics

• Publication date

  1994-05-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1093/HMG/3.5.827PMID 8081371
• 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.

• Molecular basis and consequences of a deletion in the amelogenin gene, analyzed by capture PCR.

  1993cited by this paper
• Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)

  1992cited by this paper
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  1992cited by this paper
• Genetic heterogeneity in X-linked amelogenesis imperfecta.

  1992cited by this paper
• A human X-Y homologous region encodes "amelogenin".

  1991cited by this paper
• A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1).

  1991cited by this paper
• Human and mouse amelogenin gene loci are on the sex chromosomes.

  1989cited by this paper
• Enamel hypoplasia and anomalies of the enamel.

  1975cited by this paper

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  2009cites this paper
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• [Genetic, clinical and molecular analysis of a family affected by amelogenesis imperfecta].

  2005cites this paper
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  2004cites this paper
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  2003influential citation
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  2003cites this paper
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  2002cites this paper
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  2002cites this paper
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  2001cites this paper
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  2001cites this paper
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  2001cites this paper
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  2000cites this paper
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  2000cites this paper
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  2000cites this paper
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  1999cites this paper
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  1999cites this paper
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  1999cites this paper
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  1998cites this paper
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  1998cites this paper
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  1997cites this paper
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  1997cites this paper
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  1997cites this paper
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  1997cites this paper
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  1995cites this paper
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  1995cites this paper
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  1995cites this paper
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  1995cites this paper
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  1995cites this paper
• [Molecular structure and function of matrix proteins in developing enamel--amelogenin and enamelin].

  1995cites this paper
• Understanding enamel formation from mutations causing X-linked amelogenesis imperfecta.

  1995cites this paper
• On Behalf Of: International and American Associations for Dental Research

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