Syndrome de Cohen (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Syndrome de Cohen" in French language version.

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journaldesfemmes.fr

(en) Cohen MM Jr, Hall BD, Smith DW, Graham CB, Lampert KJ « A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies » J Pediatr 1973;83:280-4. PMID 4717588
(en) Kolehmainen J, Black GC, Saarinen A, Chandler K, Clayton-Smith J, Traskelin AL, Perveen R, Kivitie-Kallio S, Norio R, Warburg M, Fryns JP, de la Chapelle A, Lehesjoki AE. « Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport » Am J Hum Genet. 2003;72:1359-69. PMID 12730828
(en) Falk MJ, Feiler HS, Neilson DE, Maxwell K, Lee JV, Segall SK, Robin NH, Wilhelmsen KC, Träskelin AL, Kolehmainen J, Lehesjoki AE, Wiznitzer M, Warman ML, « Cohen syndrome in the Ohio Amish », Am J Med Genet A, vol. 128A, n^o 1,‎ 2004, p. 23-8. (PMID 15211651) modifier

(en) Falk MJ, Feiler HS, Neilson DE, Maxwell K, Lee JV, Segall SK, Robin NH, Wilhelmsen KC, Träskelin AL, Kolehmainen J, Lehesjoki AE, Wiznitzer M, Warman ML, « Cohen syndrome in the Ohio Amish », Am J Med Genet A, vol. 128A, n^o 1,‎ 2004, p. 23-8. (PMID 15211651) modifier