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Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature.
Roscioli, T; Flanagan, S; Kumar, P; Masel, J; Gattas, M; Hyland, V J; Glass, I A.
Affiliation
  • Roscioli T; Queensland Clinical Genetics Service, Herston Hospitals Campus, Brisbane, Queensland, Australia.
Am J Med Genet ; 93(1): 22-8, 2000 Jul 03.
Article in En | MEDLINE | ID: mdl-10861678
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Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Receptors, Fibroblast Growth Factor / Receptor Protein-Tyrosine Kinases / Mutation, Missense Type of study: Diagnostic_studies / Prognostic_studies Limits: Child / Female / Humans Language: En Journal: Am J Med Genet Year: 2000 Document type: Article Affiliation country: Australia Country of publication: Estados Unidos
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Receptors, Fibroblast Growth Factor / Receptor Protein-Tyrosine Kinases / Mutation, Missense Type of study: Diagnostic_studies / Prognostic_studies Limits: Child / Female / Humans Language: En Journal: Am J Med Genet Year: 2000 Document type: Article Affiliation country: Australia Country of publication: Estados Unidos