Publications by authors named "Helene Poquet"

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Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome.
Angélique Quartier, Hélène Poquet, Brigitte Gilbert-Dussardier, Massimiliano Rossi, Anne-Sophie Casteleyn

Eur J Hum Genet· April 2017

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Transcranial Magnetic Stimulation Combined With Nicotine Replacement Therapy for Smoking Cessation: A Randomized Controlled Trial.
Benoit Trojak, Vincent Meille, Sophia Achab, Laurence Lalanne, Hélène Poquet

Brain Stimul· July 2016

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20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition.
Amélie Piton, Hélène Poquet, Claire Redin, Alice Masurel, Julia Lauer

Eur J Hum Genet· June 2014

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3q27.3 microdeletional syndrome: a recognisable clinical entity associating dysmorphic features, marfanoid habitus, intellectual disability and psychosis with mood disorder.
Julien Thevenon, Patrick Callier, Hélène Poquet, Iben Bache, Bjorn Menten

J Med Genet· January 2014

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