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Clinical Genetics|July 31, 2007
Familial CHARGE syndrome because of CHD7 mutation: clinical intra- and interfamilial variabilityA Delahaye, Y Sznajer, S Lyonnet, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Clinical spectrum of eye malformations in four patients with Mowat-Wilson syndromeA Bourchany, I Giurgea, J Thevenon, et al.
Orphanet Journal of Rare Diseases|September 23, 2020
Management of ocular involvement in the acute phase of Stevens-Johnson syndrome and toxic epidermal necrolysis: french national audit of practices, literature review, and consensus agreementD Thorel, S Ingen-Housz-Oro, G Royer, et al.
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