Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction Academic Article 2011 uri icon

authors

  • MCCABE MARK J.
  • RAZA JAMAL
  • WALKER JOANNA
  • KAVANAUGH SCOTT I.
  • TSAI PEI-SAN
  • PITTELOUD NELLY
  • MARTINEZ-BARBERA JUAN PEDRO
  • DATTANI MEHUL T.
  • GASTON-MASSUET CARLES
  • TZIAFERI VAITSA
  • GREGORY LOUSIE C:
  • ALATZOGLOU KYRIAKI S.
  • SIGNORE MASSIMO
  • DE PUELLES MARTINEZ DE LA TORRE, EDUARDO
  • GUERRELLI DIANNE
  • FAROOQI L.SADAF

publication date

  • 2011