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The International Journal of Developmental Biology|August 26, 1998
Genetic patterning of the posterior neuropore region of curly tail mouse embryos: deficiency of Wnt5a expressionF Gofflot, M Hall, G M Morriss-Kay
Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 12, 1998
Genetic patterning of the developing mouse tail at the time of posterior neuropore closureF Gofflot, M Hall, G M Morriss-Kay
Toxicology in Vitro : an International Journal Published in Association with BIBRA|July 24, 2010
Whole embryo culture of presomitic mouse embryosG Van Maele-Fabry, F Gofflot, J J Picard
Teratology|January 1, 1996
Defects in the development of branchial nerves and ganglia induced by in vitro exposure of mouse embryos to mercuric chlorideG van Maele-Fabry, F Gofflot, J J Picard
Brain Research. Developmental Brain Research|May 31, 1996
Cranial nerves and ganglia are altered after in vitro treatment of mouse embryos with valproic acid (VPA) and 4-en-VPAF Gofflot, G van Maele-Fabry, J J Picard
Journal of Anatomy|January 15, 2002
Effects of the curly tail genotype on neuroepithelial integrity and cell proliferation during late stages of primary neurulationM Hall, F Gofflot, S Iseki, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA|August 25, 2010
Developmental table of the early mouse post-implantation embryoG Van Maele-Fabry, F Delhaise, F Gofflot, et al.
Neurotoxicology and Teratology|July 1, 1995
Alterations of mouse embryonic branchial nerves and ganglia induced by ethanolG Van Maele-Fabry, F Gofflot, F Clotman, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 13, 2001
Expression of Sonic Hedgehog downstream genes is modified in rat embryos exposed in utero to a distal inhibitor of cholesterol biosynthesisF Gofflot, W Gaoua, L Bourguignon, et al.
American Journal of Medical Genetics|November 24, 1999
Absence of ventral cell populations in the developing brain in a rat model of the Smith-Lemli-Opitz syndromeF Gofflot, M Kolf-Clauw, F Clotman, et al.
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