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Expanding the phenotype for the recurrent p.Ala391Glu variant in FGFR3: Beyond crouzon syndrome and acanthosis nigricans.
Rymer, Karen; Shiang, Rita; Hsiung, Anting; Pandya, Arti; Bigdeli, Tim; Webb, Bradley T; Rhodes, Jennifer.
Affiliation
  • Rymer K; Department of Human and Molecular Genetics, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
  • Shiang R; Department of Human and Molecular Genetics, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
  • Hsiung A; Department of Human and Molecular Genetics, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
  • Pandya A; Department of Human and Molecular Genetics, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
  • Bigdeli T; Department of Psychiatry, SUNY Downstate Medical Center, Brooklyn, New York.
  • Webb BT; Department of Psychiatry, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
  • Rhodes J; Virginia Institute of Psychiatric and Behavioral Genetics, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
Mol Genet Genomic Med ; 7(6): e656, 2019 06.
Article in En | MEDLINE | ID: mdl-31016899
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Craniofacial Dysostosis / Receptor, Fibroblast Growth Factor, Type 3 / Acanthosis Nigricans Type of study: Prognostic_studies Limits: Adult / Child / Female / Humans / Infant / Male Language: En Journal: Mol Genet Genomic Med Year: 2019 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Craniofacial Dysostosis / Receptor, Fibroblast Growth Factor, Type 3 / Acanthosis Nigricans Type of study: Prognostic_studies Limits: Adult / Child / Female / Humans / Infant / Male Language: En Journal: Mol Genet Genomic Med Year: 2019 Document type: Article