Delattre O - Search Results

1

Cell-Free DNA Extracted from CSF for the Molecular Diagnosis of Pediatric Embryonal Brain Tumors.

Chicard M, Iddir Y, Masliah Planchon J, Combaret V, Attignon V, Saint-Charles A, Frappaz D, Faure-Conter C, Beccaria K, Varlet P, Geoerger B, Baulande S, Pierron G, Bouchoucha Y, Doz F, Delattre O, Waterfall JJ, Bourdeaut F, Schleiermacher G. Chicard M, et al. Among authors: delattre o. Cancers (Basel). 2023 Jul 7;15(13):3532. doi: 10.3390/cancers15133532. Cancers (Basel). 2023. PMID: 37444642 Free PMC article.

2

Two distinct deleted regions on the short arm of chromosome 1 in neuroblastoma.

Schleiermacher G, Peter M, Michon J, Hugot JP, Vielh P, Zucker JM, Magdelénat H, Thomas G, Delattre O. Schleiermacher G, et al. Among authors: delattre o. Genes Chromosomes Cancer. 1994 Aug;10(4):275-81. doi: 10.1002/gcc.2870100409. Genes Chromosomes Cancer. 1994. PMID: 7522542

3

A multiplex PCR assay for routine evaluation of deletion of the short arm of chromosome 1 in neuroblastoma.

Schleiermacher G, Peter M, Michon J, Zucker JM, Thomas G, Magdelénat H, Delattre O. Schleiermacher G, et al. Among authors: delattre o. Eur J Cancer. 1995;31A(4):535-8. doi: 10.1016/0959-8049(95)00008-7. Eur J Cancer. 1995. PMID: 7576961

4

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: delattre o. Eur J Cancer. 1996 Apr;32A(4):645-9. doi: 10.1016/0959-8049(95)00626-5. Eur J Cancer. 1996. PMID: 8695269

5

[Biological markers for the prognosis of neuroblastoma: proposal of a method of analysis].

Combaret V, Delattre O, Bénard J, Favrot MC. Combaret V, et al. Among authors: delattre o. Bull Cancer. 1998 Mar;85(3):262-6. Bull Cancer. 1998. PMID: 9752317 Free article. Review. French.

6

[Detection of micrometastases and circulating tumour cells using molecular biology technics in solid tumours].

Schleiermacher G, Delattre O. Schleiermacher G, et al. Among authors: delattre o. Bull Cancer. 2001 Jun;88(6):561-70. Bull Cancer. 2001. PMID: 11459702 Free article. French.

7

CGH analysis of secondary genetic changes in Ewing tumors: correlation with metastatic disease in a series of 43 cases.

Brisset S, Schleiermacher G, Peter M, Mairal A, Oberlin O, Delattre O, Aurias A. Brisset S, et al. Among authors: delattre o. Cancer Genet Cytogenet. 2001 Oct 1;130(1):57-61. doi: 10.1016/s0165-4608(01)00454-x. Cancer Genet Cytogenet. 2001. PMID: 11672775 Review.

8

Combined 24-color karyotyping and comparative genomic hybridization analysis indicates predominant rearrangements of early replicating chromosome regions in neuroblastoma.

Schleiermacher G, Janoueix-Lerosey I, Combaret V, Derré J, Couturier J, Aurias A, Delattre O. Schleiermacher G, et al. Among authors: delattre o. Cancer Genet Cytogenet. 2003 Feb;141(1):32-42. doi: 10.1016/s0165-4608(02)00644-1. Cancer Genet Cytogenet. 2003. PMID: 12581896

9

Variety and complexity of chromosome 17 translocations in neuroblastoma.

Schleiermacher G, Raynal V, Janoueix-Lerosey I, Combaret V, Aurias A, Delattre O. Schleiermacher G, et al. Among authors: delattre o. Genes Chromosomes Cancer. 2004 Feb;39(2):143-50. doi: 10.1002/gcc.10313. Genes Chromosomes Cancer. 2004. PMID: 14695994

10

Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma.

Trochet D, Bourdeaut F, Janoueix-Lerosey I, Deville A, de Pontual L, Schleiermacher G, Coze C, Philip N, Frébourg T, Munnich A, Lyonnet S, Delattre O, Amiel J. Trochet D, et al. Among authors: delattre o. Am J Hum Genet. 2004 Apr;74(4):761-4. doi: 10.1086/383253. Epub 2004 Mar 11. Am J Hum Genet. 2004. PMID: 15024693 Free PMC article.

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