Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1

No abstract is available for this paper.

• Publication year

  2013

• Venue

  European Journal of Human Genetics

• Publication date

  2013-11-27

• Fields of study

  Medicine

• Identifiers
  DOI 10.1038/ejhg.2013.273PMID 24281372PMCID PMC4096149
• 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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