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N-MYC amplification, loss of heterozygosity on the short arm of chromosome 1 and DNA ploidy in retinoblastoma.
Doz F, Peter M, Schleiermacher G, Vielh P, Validire P, Putterman M, Blanquet V, Desjardins L, Dufier JL, Zucker JM, Mosseri V, Thomas G, Magdelénat H, Delattre O. Doz F, et al. Among authors: blanquet v. Eur J Cancer. 1996 Apr;32A(4):645-9. doi: 10.1016/0959-8049(95)00626-5. Eur J Cancer. 1996. PMID: 8695269
alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues.
Miniou P, Jeanpierre M, Bourc'his D, Coutinho Barbosa AC, Blanquet V, Viegas-Péquignot E. Miniou P, et al. Among authors: blanquet v. Hum Genet. 1997 Jun;99(6):738-45. doi: 10.1007/s004390050441. Hum Genet. 1997. PMID: 9187666
Three novel germline mutations in exons 8 and 18 of the retinoblastoma gene.
Blanquet V, Gross MS, Turleau C, Sénamaud-Beaufort C, Doz F, Besmond C. Blanquet V, et al. Hum Mol Genet. 1994 Jul;3(7):1185-6. doi: 10.1093/hmg/3.7.1185. Hum Mol Genet. 1994. PMID: 7981694 No abstract available.
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.
Miniou P, Jeanpierre M, Blanquet V, Sibella V, Bonneau D, Herbelin C, Fischer A, Niveleau A, Viegas-Péquignot E. Miniou P, et al. Among authors: blanquet v. Hum Mol Genet. 1994 Dec;3(12):2093-102. doi: 10.1093/hmg/3.12.2093. Hum Mol Genet. 1994. PMID: 7881405
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