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Page 1
Exome sequencing identifies the first genetic determinants of sirenomelia in humans.
Lecoquierre F, Brehin AC, Coutant S, Coursimault J, Bazin A, Finck W, Benoist G, Begorre M, Beneteau C, Cailliez D, Chenal P, De Jong M, Degré S, Devisme L, Francannet C, Gérard B, Jeanne C, Joubert M, Journel H, Laurichesse Delmas H, Layet V, Liquier A, Mangione R, Patrier S, Pelluard F, Petit F, Tillouche N, van Ravenswaaij-Arts C, Frebourg T, Saugier-Veber P, Gruchy N, Nicolas G, Gerard M. Lecoquierre F, et al. Among authors: cailliez d. Hum Mutat. 2020 May;41(5):926-933. doi: 10.1002/humu.23998. Epub 2020 Mar 1. Hum Mutat. 2020. PMID: 32058622
Sirenomelia and caudal malformations in two families.
Gerard M, Layet V, Costa T, Roumazeilles Y, Chenal P, Cailliez D, Gerard B. Gerard M, et al. Among authors: cailliez d. Am J Med Genet A. 2012 Jul;158A(7):1801-7. doi: 10.1002/ajmg.a.35408. Epub 2012 Apr 20. Am J Med Genet A. 2012. PMID: 22522670
[Sarcoidosis and goiter. A case report in an adolescent].
Dumesnil C, Le Roux P, Duquenoy A, Cailliez D, Le Luyer B. Dumesnil C, et al. Among authors: cailliez d. Arch Pediatr. 2000 Aug;7(8):847-50. doi: 10.1016/S0929-693X(00)80195-5. Arch Pediatr. 2000. PMID: 10985186 French.
[Bullous mastocytosis in infancy: a rare presentation].
Deverrière G, Carré D, Nae I, Cailliez D, Boulloche J. Deverrière G, et al. Among authors: cailliez d. Arch Pediatr. 2012 Jul;19(7):722-5. doi: 10.1016/j.arcped.2012.04.021. Epub 2012 Jun 2. Arch Pediatr. 2012. PMID: 22664234 French.
[Cutaneous schistosomiasis. Apropos of a case].
Mathelier-Fusade P, Beaulieu-Lacoste I, Cailliez D, Audebert C. Mathelier-Fusade P, et al. Among authors: cailliez d. Ann Dermatol Venereol. 1991;118(10):715-7. Ann Dermatol Venereol. 1991. PMID: 1781591 French. No abstract available.