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Clinical interest of molecular study in cases of isolated midline craniosynostosis.
Di Rocco, Federico; Rossi, Massimiliano; Verlut, Isabelle; Szathmari, Alexandru; Beuriat, Pierre Aurélien; Chatron, Nicolas; Chauvel-Picard, Julie; Mottolese, Carmine; Monin, Pauline; Vinchon, Matthieu; Guernouche, Sofia; Collet, Corinne.
Afiliação
  • Di Rocco F; Department of Pediatric Neurosurgery, French Referral Center for Craniosynostosis, Hôpital Femme Mère-Enfant Hospices Civils de Lyon, University of Lyon, INSERM 1033, Lyon, France.
  • Rossi M; Department of Genetics, Lyon University Hospitals, INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, Lyon, France.
  • Verlut I; Department of Pediatric Neurosurgery, French Referral Center for Craniosynostosis, Hôpital Femme Mère-Enfant Hospices Civils de Lyon, University of Lyon, INSERM 1033, Lyon, France.
  • Szathmari A; Department of Pediatric Neurosurgery, French Referral Center for Craniosynostosis, Hôpital Femme Mère-Enfant Hospices Civils de Lyon, University of Lyon, INSERM 1033, Lyon, France.
  • Beuriat PA; Department of Pediatric Neurosurgery, French Referral Center for Craniosynostosis, Hôpital Femme Mère-Enfant Hospices Civils de Lyon, University of Lyon, INSERM 1033, Lyon, France.
  • Chatron N; Department of Genetics, Lyon University Hospitals, INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, Lyon, France.
  • Chauvel-Picard J; Department of Pediatric Cranio-Maxillo-Facial Surgery, Hôpital Femme Mère Enfant, Université Claude Bernard Lyon 1, Lyon, France.
  • Mottolese C; Department of Pediatric Neurosurgery, French Referral Center for Craniosynostosis, Hôpital Femme Mère-Enfant Hospices Civils de Lyon, University of Lyon, INSERM 1033, Lyon, France.
  • Monin P; Department of Genetics, Lyon University Hospitals, INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, Lyon, France.
  • Vinchon M; Department of Pediatric Neurosurgery, French Referral Center for Craniosynostosis, Hôpital Femme Mère-Enfant Hospices Civils de Lyon, University of Lyon, INSERM 1033, Lyon, France.
  • Guernouche S; Department of Pediatric Neurosurgery, French Referral Center for Craniosynostosis, Hôpital Femme Mère-Enfant Hospices Civils de Lyon, University of Lyon, INSERM 1033, Lyon, France.
  • Collet C; Department of Genetics, Robert Debré Hospital, Inserm 1132, Université de Paris Cité, Paris, France. corinne.collet@aphp.fr.
Eur J Hum Genet ; 31(6): 621-628, 2023 06.
Article em En | MEDLINE | ID: mdl-36732661
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Craniossinostoses Tipo de estudo: Diagnostic_studies Limite: Child / Child, preschool / Humans / Infant Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Craniossinostoses Tipo de estudo: Diagnostic_studies Limite: Child / Child, preschool / Humans / Infant Idioma: En Ano de publicação: 2023 Tipo de documento: Article