Novel mutation in the FGFR2 gene at the same codon as the Crouzon syndrome mutations in a severe Pfeiffer syndrome type 2 case.

No abstract is available for this paper.

• Publication year

  1998

• Venue

  American journal of medical genetics

• Publication date

  1998-01-23

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/(SICI)1096-8628(19980123)75:3<252::AID-AJMG4>3.0.CO;2-SPMID 9475591
• 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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