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Page 1
Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis.
Martignetti JA, Tian L, Li D, Ramirez MC, Camacho-Vanegas O, Camacho SC, Guo Y, Zand DJ, Bernstein AM, Masur SK, Kim CE, Otieno FG, Hou C, Abdel-Magid N, Tweddale B, Metry D, Fournet JC, Papp E, McPherson EW, Zabel C, Vaksmann G, Morisot C, Keating B, Sleiman PM, Cleveland JA, Everman DB, Zackai E, Hakonarson H. Martignetti JA, et al. Among authors: morisot c. Am J Hum Genet. 2013 Jun 6;92(6):1001-7. doi: 10.1016/j.ajhg.2013.04.024. Epub 2013 May 23. Am J Hum Genet. 2013. PMID: 23731542 Free PMC article.
[Jejunal atresia and persistent mullerian duct syndrome].
Klosowski S, Abriak A, Morisot C, Bayart HC, Belville C, Thelliez P, Gottrand F, Croquette MF, Deroubaix P. Klosowski S, et al. Among authors: morisot c. Arch Pediatr. 1997 Dec;4(12):1264-5. doi: 10.1016/s0929-693x(97)82624-3. Arch Pediatr. 1997. PMID: 9538438 French. No abstract available.
[Congenital pulmonary lymphangiectasia revealed by cardiac arrest].
Bachiri A, Djebara A, Klosowski S, Haouari N, Thelliez P, Voisin O, Devisme L, Morisot C. Bachiri A, et al. Among authors: morisot c. Arch Pediatr. 2003 Jul;10(7):615-8. doi: 10.1016/s0929-693x(03)00280-x. Arch Pediatr. 2003. PMID: 12907069 French.
[Unusual mechanism in Prader-Willi syndrome: incidence in genetic counseling].
Klosowski S, Delobel B, Morisot C, Kongolo G, Biancalana V, Thelliez P, Djebara A, Croquette MF, Deroubaix P. Klosowski S, et al. Among authors: morisot c. Arch Pediatr. 1998 Aug;5(8):934-5. doi: 10.1016/s0929-693x(98)80208-x. Arch Pediatr. 1998. PMID: 9759307 French. No abstract available.
28 results