Moutou C - Search Results

1

Cancers in relatives of children with non-Hodgkin's lymphoma.

Le Bihan C, Moutou C, Chompret A, Abel A, Poisson N, Brugières L, Lemerle J, Bonaïti-Pelliè C. Le Bihan C, et al. Among authors: moutou c. Leuk Res. 1996 Feb;20(2):181-6. doi: 10.1016/0145-2126(95)00138-7. Leuk Res. 1996. PMID: 8628018

2

The French Wilms' tumour study: no clear evidence for cancer prone families.

Moutou C, Hochez J, Chompret A, Tournade MF, Le Bihan C, Zucker JM, Lemerle J, Bonaïti-Pellié C. Moutou C, et al. J Med Genet. 1994 Jun;31(6):429-34. doi: 10.1136/jmg.31.6.429. J Med Genet. 1994. PMID: 8071968 Free PMC article.

3

Screening for germ line p53 mutations in children with malignant tumors and a family history of cancer.

Brugières L, Gardes M, Moutou C, Chompret A, Meresse V, Martin A, Poisson N, Flamant F, Bonaïti-Pellié C, Lemerle J, et al. Brugières L, et al. Among authors: moutou c. Cancer Res. 1993 Feb 1;53(3):452-5. Cancer Res. 1993. PMID: 8425176

4

Genetic transmission of susceptibility to cancer in families of children with soft tissue sarcomas.

Moutou C, Le Bihan C, Chompret A, Poisson N, Brugières L, Bressac B, Feunteun J, Lemerle J, Bonaïti-Pellié C. Moutou C, et al. Cancer. 1996 Oct 1;78(7):1483-91. doi: 10.1002/(sici)1097-0142(19961001)78:7<1483::aid-cncr16>3.0.co;2-w. Cancer. 1996. PMID: 8839555

5

Genetics and epidemiology of Wilms' tumor: the French Wilms' tumor study.

Bonaïti-Pellié C, Chompret A, Tournade MF, Hochez J, Moutou C, Zucker JM, Steschenko D, Brunat-Mentigny M, Roché H, Tron P, et al. Bonaïti-Pellié C, et al. Among authors: moutou c. Med Pediatr Oncol. 1992;20(4):284-91. doi: 10.1002/mpo.2950200404. Med Pediatr Oncol. 1992. PMID: 1318995

6

ARCAD: a method for estimating age-dependent disease risk associated with mutation carrier status from family data.

Le Bihan C, Moutou C, Brugières L, Feunteun J, Bonaïti-Pellié C. Le Bihan C, et al. Among authors: moutou c. Genet Epidemiol. 1995;12(1):13-25. doi: 10.1002/gepi.1370120103. Genet Epidemiol. 1995. PMID: 7713397

7

Testing genomic imprinting in Wilm's tumor.

Moutou C, Chompret A, Hochez J, Tournade MF, Zucker JM, Lemerle J, Junien C, Bonaïti-Pellié C. Moutou C, et al. Eur J Hum Genet. 1993;1(3):190-205. doi: 10.1159/000472413. Eur J Hum Genet. 1993. PMID: 8044646

8

Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.

Moutou C, Junien C, Henry I, Bonaïti-Pellié C. Moutou C, et al. J Med Genet. 1992 Apr;29(4):217-20. doi: 10.1136/jmg.29.4.217. J Med Genet. 1992. PMID: 1583638 Free PMC article.

9

Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic.

Moutou C, Vincent MC, Biancalana V, Mandel JL. Moutou C, et al. Hum Mol Genet. 1997 Jul;6(7):971-9. doi: 10.1093/hmg/6.7.971. Hum Mol Genet. 1997. PMID: 9215664

10

Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis.

Moutou C, Gardes N, Viville S. Moutou C, et al. Eur J Hum Genet. 2002 Apr;10(4):231-8. doi: 10.1038/sj.ejhg.5200794. Eur J Hum Genet. 2002. PMID: 12032730

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