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Co-occurrence of frameshift mutations in SMAD6 and TCF12 in a child with complex craniosynostosis.
Timberlake, Andrew T; Wu, Robin; Nelson-Williams, Carol; Furey, Charuta G; Hildebrand, Kristi I; Elton, Scott W; Wood, Jeyhan S; Persing, John A; Lifton, Richard P.
Afiliação
  • Timberlake AT; 1Department of Genetics, Yale University School of Medicine, New Haven, CT USA.
  • Wu R; 2Section of Plastic and Reconstructive Surgery, Yale University School of Medicine, New Haven, CT USA.
  • Nelson-Williams C; 2Section of Plastic and Reconstructive Surgery, Yale University School of Medicine, New Haven, CT USA.
  • Furey CG; 1Department of Genetics, Yale University School of Medicine, New Haven, CT USA.
  • Hildebrand KI; 1Department of Genetics, Yale University School of Medicine, New Haven, CT USA.
  • Elton SW; 3Division of Pediatric Neurosurgery, University of North Carolina School of Medicine, Chapel Hill, NC USA.
  • Wood JS; 3Division of Pediatric Neurosurgery, University of North Carolina School of Medicine, Chapel Hill, NC USA.
  • Persing JA; 4Division of Plastic and Reconstructive Surgery, University of North Carolina School of Medicine, Chapel Hill, NC USA.
  • Lifton RP; 2Section of Plastic and Reconstructive Surgery, Yale University School of Medicine, New Haven, CT USA.
Hum Genome Var ; 5: 14, 2018.
Article em En | MEDLINE | ID: mdl-30038786
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hum Genome Var Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hum Genome Var Ano de publicação: 2018 Tipo de documento: Article