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Nature Genetics|June 3, 2000
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndromeS Chavanas, C Bodemer, A Rochat, et al.La Nouvelle Presse Medicale|May 16, 1981
[Skin lesions in systemic candidiasis (author's transl)]Y de Prost, P Rondeau, J P Vernant, et al.La Revue Du Praticien|October 27, 1997
[Febrile eruptions in systemic diseases in children]D Hamel-Teillac, C BodemerAnnales De Dermatologie Et De Venereologie|December 3, 2014
[Acanthosis nigricans in children and Crouzon syndrome]M Lagaude, M Barreau, M Jokic, et al.Journal of Medical Genetics|November 6, 2001
Hirschsprung disease, associated syndromes, and genetics: a reviewJ Amiel, S LyonnetArchives Des Maladies Du Coeur Et Des Vaisseaux|July 1, 1979
[Fiessinger-Leroy-Reiter syndrome with non-obstructive cardiomyopathy treated with methotrexate]O Blétry, Y De Prost, C Scheuble, et al.Nature Genetics|November 4, 2000
Mutant WD-repeat protein in triple-A syndromeA Tullio-Pelet, R Salomon, S Hadj-Rabia, et al.Annales De Dermatologie Et De Venereologie|January 1, 1995
[Ultrastructural study of hereditary benign telangiectasia. Differential diagnosis from Osler Rendu disease]P Tsianakas, D Teillac-Hamel, S Fraitag, et al.La Nouvelle Presse Medicale|October 25, 1975
[The blood chloride-phosphorus ratio in the diagnosis of hyperparathyroidism. 31 parathyroid adenomas]J P Fendler, Y de Prost, G Dongradi, et al.Annales De Dermatologie Et De Venereologie|June 11, 2002
[Facial cellulite associated with mandibular osteomyelitis in an infant]M Bertocchi, D Hamel-Teillac, S Emond, et al.Pageof 38