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When sporadic disease is not sporadic: the potential for genetic etiology.
Arch Neurol. 2004 Feb;61(2):213-6. doi: 10.1001/archneur.61.2.213.
Arch Neurol. 2004.
PMID: 14967768
Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2.
Rapley EA, Barfoot R, Bonaïti-Pellié C, Chompret A, Foulkes W, Perusinghe N, Reeve A, Royer-Pokora B, Schumacher V, Shelling A, Skeen J, de Tourreil S, Weirich A, Pritchard-Jones K, Stratton MR, Rahman N.
Rapley EA, et al. Among authors: de tourreil s.
Br J Cancer. 2000 Jul;83(2):177-83. doi: 10.1054/bjoc.2000.1283.
Br J Cancer. 2000.
PMID: 10901367
Free PMC article.
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Spinobulbar muscular atrophy: polyglutamine-expanded androgen receptor is proteolytically resistant in vitro and processed abnormally in transfected cells.
Abdullah A, Trifiro MA, Panet-Raymond V, Alvarado C, de Tourreil S, Frankel D, Schipper HM, Pinsky L.
Abdullah A, et al. Among authors: de tourreil s.
Hum Mol Genet. 1998 Mar;7(3):379-84. doi: 10.1093/hmg/7.3.379.
Hum Mol Genet. 1998.
PMID: 9466993
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