Doz F - Search Results

1

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. Among authors: doz f. 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.

2

Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma.

Blanquet V, Turleau C, Gross-Morand MS, Sénamaud-Beaufort C, Doz F, Besmond C. Blanquet V, et al. Among authors: doz f. Hum Mol Genet. 1995 Mar;4(3):383-8. doi: 10.1093/hmg/4.3.383. Hum Mol Genet. 1995. PMID: 7795591

3

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

4

Retinoblastoma.

Zucker JM, Desjardins L, Doz F. Zucker JM, et al. Among authors: doz f. Eur J Cancer. 1998 Jun;34(7):1045-8; discussion 1048-9. doi: 10.1016/s0959-8049(98)00181-6. Eur J Cancer. 1998. PMID: 9849453 Review. No abstract available.

5

Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletion.

Baud O, Cormier-Daire V, Lyonnet S, Desjardins L, Turleau C, Doz F. Baud O, et al. Among authors: doz f. Clin Genet. 1999 Jun;55(6):478-82. doi: 10.1034/j.1399-0004.1999.550614.x. Clin Genet. 1999. PMID: 10450867

6

The survival gene MED4 explains low penetrance retinoblastoma in patients with large RB1 deletion.

Dehainault C, Garancher A, Castéra L, Cassoux N, Aerts I, Doz F, Desjardins L, Lumbroso L, Montes de Oca R, Almouzni G, Stoppa-Lyonnet D, Pouponnot C, Gauthier-Villars M, Houdayer C. Dehainault C, et al. Among authors: doz f. Hum Mol Genet. 2014 Oct 1;23(19):5243-50. doi: 10.1093/hmg/ddu245. Epub 2014 May 23. Hum Mol Genet. 2014. PMID: 24858910

7

Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome.

Viot-Szoboszlai G, Amiel J, Doz F, Prieur M, Couturier J, Zucker JN, Henry I, Munnich A, Vekemans M, Lyonnet S. Viot-Szoboszlai G, et al. Among authors: doz f. Clin Genet. 1998 Apr;53(4):278-80. doi: 10.1111/j.1399-0004.1998.tb02696.x. Clin Genet. 1998. PMID: 9650765

8

Multiple acral fibromas in a patient with familial retinoblastoma: a cutaneous marker of tumour-suppressor gene germline mutation?

Dereure O, Savoy D, Doz F, Junien C, Guilhou JJ. Dereure O, et al. Among authors: doz f. Br J Dermatol. 2000 Oct;143(4):856-9. doi: 10.1046/j.1365-2133.2000.03790.x. Br J Dermatol. 2000. PMID: 11069472

9

Osteosarcoma following retinoblastoma: age at onset and latency period.

Chauveinc L, Mosseri V, Quintana E, Desjardins L, Schlienger P, Doz F, Dutrillaux B. Chauveinc L, et al. Among authors: doz f. Ophthalmic Genet. 2001 Jun;22(2):77-88. doi: 10.1076/opge.22.2.77.2228. Ophthalmic Genet. 2001. PMID: 11449317 Review.

10

Comprehensive screening for constitutional RB1 mutations by DHPLC and QMPSF.

Houdayer C, Gauthier-Villars M, Laugé A, Pagès-Berhouet S, Dehainault C, Caux-Moncoutier V, Karczynski P, Tosi M, Doz F, Desjardins L, Couturier J, Stoppa-Lyonnet D. Houdayer C, et al. Among authors: doz f. Hum Mutat. 2004 Feb;23(2):193-202. doi: 10.1002/humu.10303. Hum Mutat. 2004. PMID: 14722923

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

318 results

Search Page