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Delineating the phenotypic spectrum of FOXG1 syndrome: from congenital microcephaly to hyperkinetic encephalopathy.
Delineating the phenotypic spectrum of FOXG1 syndrome: from congenital microcephaly to hyperkinetic encephalopathy.
2018
Nancy Vegas
Camille Maillard
Nathalie Boddaert
Joseph Toulouse
Elise Schaefer
Tally Lerman-Sagie
Dorit Lev
Barth Magalie
Sébastien Moutton
Eric Haan
Bertrand Isidor
Delphine Héron
Mathieu Milh
Stéphane Rondeau
Caroline Michot
Stéphanie Valence
Sabrina Wagner
Marie Hully
Cyril Mignot
Alice Masurel
Alexandre N. Datta
Sylvie Odent
Mathilde Nizon
Leila Lazaro
Marie Vincent
Benjamin Cogné
Anne-Marie Guerrot
Stéphanie Arpin
Jean-Michel Pedespan
Isabelle Caubel
Bénédicte Pontier
Baptiste Troude
François Rivier
Christophe Philippe
Thierry Bienvenu
Marie-Aude Spitz
Amandine Bery
Nadia Bahi-Buisson
Keywords:
Congenital microcephaly
Encephalopathy
Pediatrics
Phenotype
FOXG1 syndrome
Medicine
Correction
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