38412-3

LOINC 2.82

FGFR2 gene targeted mutation analysis in Blood or Tissue by Molecular genetics method

FGFR2 gene Mut Anl Bld/T

Component

  • FGFR2 gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Find

Scale

  • Doc

Method

  • Molgen

Related names

  • Bacteria expressed kinase; BBDS; BEK; BFR-1; Blood; CD332; CEK3; CFD1; Craniofacial dysostosis 1; Crouzon syndrome; Document; ECT1; Fibroblast growth factor receptor 2; Finding; Findings; Genetics; Heredity; Heritable; Inherited; Jackson-Weiss syndrome; JWS; Keratinocyte growth factor receptor; KGFR; K-SAM; KSAM-1; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; PCR; Pfeiffer syndrome; Point in time; Random; Tissue; Tissue, unspecified; TK14; TK25; WB; Whole blood; Whole blood or Tissue

Index terms

  • Bacteria expressed kinase
  • BBDS
  • BEK
  • BFR-1
  • Blood
  • CD332
  • CEK3
  • CFD1
  • Craniofacial dysostosis 1
  • Crouzon syndrome
  • Document
  • ECT1
  • Fibroblast growth factor receptor 2
  • Finding
  • Findings
  • Genetics
  • Heredity
  • Heritable
  • Inherited
  • Jackson-Weiss syndrome
  • JWS
  • K-SAM
  • Keratinocyte growth factor receptor
  • KGFR
  • KSAM-1
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Anl
  • Mutations
  • PCR
  • Pfeiffer syndrome
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • TK14
  • TK25

3 further terms