Heather Etchevers: all publications

• Publications

  • de Pontual L, Trochet D, Bourdeaut F, Thomas S, Etchevers H, Chompret A, Minard V, Valteau D, Brugieres L, Munnich A, Delattre O, Lyonnet S, Janoueix-Lerosey I, Amiel J. Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma. European journal of cancer (Oxford, England : 1990) 43 (16) , 2366-72 (2007) (Epub 31 Aug 2007) PubMed ID:(17765533)

  • Golzio C, Martinovic-Bouriel J, Thomas S, Mougou-Zrelli S, Grattagliano-Bessieres B, Bonniere M, Delahaye S, Munnich A, Encha-Razavi F, Lyonnet S, Vekemans M, Attie-Bitach T, Etchevers H. Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6. American journal of human genetics 80 (6) , 1179-87 (2007) (Epub 11 Apr 2007) PubMed ID:(17503335)

  • Etchevers H, Amiel J, Lyonnet S. Molecular bases of human neurocristopathies. Advances in experimental medicine and biology 589 , 213-34 (2006) PubMed ID:(17076285)

  • Etchevers H, Vincent C, Le Douarin N, Couly G. The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain. Development (Cambridge, England) 128 (7) , 1059-68 (2001) PubMed ID:(11245571)

  • Etchevers H, Couly G, Vincent C, Le Douarin N. Anterior cephalic neural crest is required for forebrain viability. Development (Cambridge, England) 126 (16) , 3533-43 (1999) PubMed ID:(10409500)

  • Detrait E, George T, Etchevers H, Gilbert J, Vekemans M, Speer M. Human neural tube defects: developmental biology, epidemiology, and genetics. Neurotoxicology and teratology 27 (3) , 515-24 (Epub 05 Mar 2005) PubMed ID:(15939212)