Valérie Raclin
Hôpitaux Universitaires Henri-Mondor(FR)
Publications by Year
Research Areas
RNA modifications and cancer, Neurogenetic and Muscular Disorders Research, Microtubule and mitosis dynamics, Genomic variations and chromosomal abnormalities, Congenital Anomalies and Fetal Surgery
Most-Cited Works
- → TP63 gene mutation in ADULT syndrome(2001)98 cited
- → Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.(1996)92 cited
- → Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature(1998)57 cited
- → A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmenti(2004)50 cited
- → Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature(1999)42 cited
- → Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.(1992)33 cited
- → Prenatal diagnosis of respiratory chain deficiency by direct mutation screening(2001)15 cited
- → De novo deletions in spinal muscular atrophy: implications for genetic counselling.(1997)14 cited
- → Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areas(2012)10 cited
- → The enlarging spectrum of Nav1.7 mutations associated with neurological pain syndromes. (P2.022)(2015)1 cited