Publications by authors named "Charles Decaestecker"

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Delineation of EFTUD2 haploinsufficiency-related phenotypes through a series of 36 patients.
Daphné Lehalle, Christopher T Gordon, Myriam Oufadem, Géraldine Goudefroye, Lucile Boutaud, Charles Decaestecker

Hum Mutat· April 2014

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EFTUD2 haploinsufficiency leads to syndromic oesophageal atresia.
Christopher T Gordon, Florence Petit, Myriam Oufadem, Charles Decaestecker, Anne-Sophie Jourdain

J Med Genet· December 2012

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