Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; a consensus statement from the European Reference Network for Congenital Malformations and Intellectual Disability - Archive ouverte HAL Access content directly
Journal Articles Orphanet Journal of Rare Diseases Year : 2019

Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; a consensus statement from the European Reference Network for Congenital Malformations and Intellectual Disability

John Dean
  • Function : Author
Hubert Journel
  • Function : Author
Amanda Wood
  • Function : Author
Janet Williams
  • Function : Author
Verna Cuthbert
  • Function : Author
Latha Hackett
  • Function : Author
Neelo Aslam
  • Function : Author
Gregory James
  • Function : Author
Lena Westbom
  • Function : Author
Ruth Day
  • Function : Author
Edmund Ladusans
  • Function : Author
Adam Jackson
Iain Bruce
  • Function : Author
Robert Walker
  • Function : Author
Sangeet Sidhu
  • Function : Author
Catrina Dyer
  • Function : Author
Jane Ashworth
  • Function : Author
Daniel Hindley
  • Function : Author
Gemma Arca Diaz
  • Function : Author
Myfanwy Rawson
  • Function : Author
Peter Turnpenny
  • Function : Author
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Dates and versions

hal-02277996 , version 1 (07-07-2020)

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Jill Clayton-Smith, Rebecca Bromley, John Dean, Hubert Journel, Sylvie Odent, et al.. Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; a consensus statement from the European Reference Network for Congenital Malformations and Intellectual Disability. Orphanet Journal of Rare Diseases, 2019, 14 (1), pp.180. ⟨10.1186/s13023-019-1064-y⟩. ⟨hal-02277996⟩
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