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Clinical, genetic and neuropathological findings in a series of 138 fetuses with a corpus callosum malformation.
Alby, Caroline; Malan, Valérie; Boutaud, Lucile; Marangoni, Maria Angela; Bessières, Bettina; Bonniere, Maryse; Ichkou, Amale; Elkhartoufi, Nadia; Bahi-Buisson, Nadia; Sonigo, Pascale; Millischer, Anne-Elodie; Thomas, Sophie; Ville, Yves; Vekemans, Michel; Encha-Razavi, Férechté; Attié-Bitach, Tania.
Afiliação
  • Alby C; INSERM U1163, Institut Imagine, Hôpital Necker-Enfants Malades.
  • Malan V; Service de Gynécologie-Obstétrique, Hôpital Necker-Enfants Malades, APHP, Paris, France.
  • Boutaud L; INSERM U1163, Institut Imagine, Hôpital Necker-Enfants Malades.
  • Marangoni MA; Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, APHP, Paris, France.
  • Bessières B; Université Paris Descartes, Paris Sorbonne Cité
  • Bonniere M; INSERM U1163, Institut Imagine, Hôpital Necker-Enfants Malades.
  • Ichkou A; Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, APHP, Paris, France.
  • Elkhartoufi N; Université Paris Descartes, Paris Sorbonne Cité
  • Bahi-Buisson N; Service de Gynécologie-Obstétrique, Hôpital Necker-Enfants Malades, APHP, Paris, France.
  • Sonigo P; Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, APHP, Paris, France.
  • Millischer AE; Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, APHP, Paris, France.
  • Thomas S; Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, APHP, Paris, France.
  • Ville Y; Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, APHP, Paris, France.
  • Vekemans M; INSERM U1163, Institut Imagine, Hôpital Necker-Enfants Malades.
  • Encha-Razavi F; Université Paris Descartes, Paris Sorbonne Cité
  • Attié-Bitach T; Service de Neuropédiatrie, Hôpital Necker-Enfants Malades, APHP, Paris, France.
Birth Defects Res A Clin Mol Teratol ; 106(1): 36-46, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26663670
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aberrações Cromossômicas / Corpo Caloso / Agenesia do Corpo Caloso / Mutação / Proteínas do Tecido Nervoso Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Pregnancy Idioma: En Revista: Birth Defects Res A Clin Mol Teratol Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aberrações Cromossômicas / Corpo Caloso / Agenesia do Corpo Caloso / Mutação / Proteínas do Tecido Nervoso Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Pregnancy Idioma: En Revista: Birth Defects Res A Clin Mol Teratol Ano de publicação: 2016 Tipo de documento: Article