Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 gene

Clinical Genetics

Volumn 58, Issue 1, 2000, Pages 81-83

  Priolo, M ^a   Lerone, M ^a   Baffico, M ^a   Baldi, M ^a   Ravazzolo, R ^a   Cama, A ^a   Capra, V ^a   Silengo, M ^a  

^a G GASLINI INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; FIBROBLAST GROWTH FACTOR RECEPTOR;

ACROCEPHALOSYNDACTYLY; CASE REPORT; CRANIOFACIAL SYNOSTOSIS; GENE MUTATION; HUMAN; LETTER; MALE; PRIORITY JOURNAL; RECEPTOR GENE;

ACROCEPHALOSYNDACTYLIA; AMINO ACID SEQUENCE; DNA MUTATIONAL ANALYSIS; HUMANS; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RECEPTORS, FIBROBLAST GROWTH FACTOR; SEQUENCE DELETION;

EID: 0033924956     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2000.580116.x     Document Type: Letter

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