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Page 1
Alternative pathways of MYCN gene copy number increase in primary neuroblastoma tumors.
Valent A, Guillaud-Bataille M, Farra C, Lozach F, Spengler B, Terrier-Lacombe MJ, Valteau-Couanet D, Danglot G, Lenoir GM, Brison O, Bénard J, Bernheim A. Valent A, et al. Among authors: lenoir gm. Cancer Genet Cytogenet. 2004 Aug;153(1):10-5. doi: 10.1016/j.cancergencyto.2003.12.007. Cancer Genet Cytogenet. 2004. PMID: 15325088
Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma.
Laud K, Marian C, Avril MF, Barrois M, Chompret A, Goldstein AM, Tucker MA, Clark PA, Peters G, Chaudru V, Demenais F, Spatz A, Smith MW, Lenoir GM, Bressac-de Paillerets B; French Hereditary Melanoma Study Group. Laud K, et al. Among authors: lenoir gm. J Med Genet. 2006 Jan;43(1):39-47. doi: 10.1136/jmg.2005.033498. Epub 2005 Jun 3. J Med Genet. 2006. PMID: 15937071 Free PMC article.
Molecular detection of early-stage laryngopharyngeal squamous cell carcinomas.
Temam S, Bénard J, Dugas C, Trassard M, Gormally E, Soria JC, Faivre S, Luboinski B, Marandas P, Hainaut P, Lenoir G, Mao L, Janot F. Temam S, et al. Among authors: lenoir g. Clin Cancer Res. 2005 Apr 1;11(7):2547-51. doi: 10.1158/1078-0432.CCR-04-1535. Clin Cancer Res. 2005. PMID: 15814632
Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients.
Kannengiesser C, Brookes S, del Arroyo AG, Pham D, Bombled J, Barrois M, Mauffret O, Avril MF, Chompret A, Lenoir GM, Sarasin A; French Hereditary Melanoma Study Group; Peters G, Bressac-de Paillerets B. Kannengiesser C, et al. Among authors: lenoir gm. Hum Mutat. 2009 Apr;30(4):564-74. doi: 10.1002/humu.20845. Hum Mutat. 2009. PMID: 19260062
652 results