Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndrome.

No abstract is available for this paper.

• Publication year

  2005

• Venue

  Chinese Medical Journal

• Publication date

  2005-09-20

• Fields of study

  Medicine

• Identifiers
  PMID 16232326
• 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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  2005cited by this paper
• Sotos syndrome common deletion is mediated by directly oriented subunits within inverted Sos-REP low-copy repeats.

  2005cited by this paper
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• Genotype-Phenotype Correlation in Patients Suspected of Having Sotos Syndrome

  2004cited by this paper
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  2004cited by this paper
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  2003cited by this paper
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  2003cited by this paper
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  2003cited by this paper
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  2003cited by this paper
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  2003cited by this paper
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  2002cited by this paper
• Molecular characterization of NSD1, a human homologue of the mouse Nsd1 gene.

  2001cited by this paper
• Growing interest in overgrowth

  1998cited by this paper
• Two distinct nuclear receptor interaction domains in NSD1, a novel SET protein that exhibits characteristics of both corepressors and coactivators

  1998cited by this paper
• The syndromes of Sotos and Weaver: reports and review.

  1998cited by this paper
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  1994cited by this paper
• Weaver syndrome.

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