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The British Journal of Dermatology|May 11, 2013
Propranolol-resistant infantile haemangiomasS Caussé, H Aubert, M Saint-Jean, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1996
[Genetics of Hirschsprung disease]T Attié, R Salomon, J Amiel, et al.
Annals of Neurology|October 12, 2000
Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutationV Pingault, A Guiochon-Mantel, N Bondurand, et al.
American Journal of Medical Genetics|January 20, 1997
Microsatellite DNA markers detects 95% of chromosome 22q11 deletionsD Bonnet, V Cormier-Daire, J Kachaner, et al.
Pediatric Radiology|November 3, 1998
Presentation of six cases of Stüve-Wiedemann syndromeV Cormier-Daire, A Munnich, S Lyonnet, et al.
Presse Medicale (Paris, France : 1983)|May 23, 1987
[Visceral lesions in hypereosinophilia]L Prin, O Blétry, A B Tonnel, et al.
The Journal of Clinical Investigation|August 1, 1994
Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophyB Fournier, J M Saudubray, B Benichou, et al.
Oncogene Research|July 1, 1987
Expression of c-myc is under dietary control in rat liverD Corcos, S Vaulont, N Denis, et al.
L'Encephale|November 25, 2018
[Child psychiatry interventions in patients with 22q11 deletion syndrome: From treatment to prevention]A Novo, L Woestelandt, B Rousselot-Pailley, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 1, 1996
[Isolated neonatal dysfunction of brainstem]V Abadie, G Chéron, S Lyonnet, et al.
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