ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome

No abstract is available for this paper.

• Publication year

  2011

• Venue

  European Journal of Human Genetics

• Publication date

  2011-11-09

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/ejhg.2011.195PMID 22071890PMCID PMC3283184
• 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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