Analysis of the mutational spectrum of the FGFR2 gene in Pfeiffer syndrome

Human Genetics

Volumn 104, Issue 5, 1999, Pages 425-431

  Cornejo Roldan, Laura R ^a,c   Roessler, Erich ^a   Muenke, Maximilian ^a,b  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c UNIVERSIDAD AUTÓNOMA DEL ESTADO DE HIDALGO   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTEINE; FIBROBLAST GROWTH FACTOR RECEPTOR;

ACROCEPHALOSYNDACTYLY; ARTICLE; CODON; DNA SEQUENCE; EXON; GENE MUTATION; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

ACROCEPHALOSYNDACTYLIA; ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; CODON; CYSTEINE; EXONS; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; MUTATION, MISSENSE; POINT MUTATION; PROTEIN CONFORMATION; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 1; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RECEPTORS, FIBROBLAST GROWTH FACTOR;

EID: 0032992570     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050979     Document Type: Article

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