Similar articles for PMID: 14670928

Year	Number of Results
1982	1
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1997	1
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2003	6
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2007	3
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2024	0

1

Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood.

Hirsch B, Shimamura A, Moreau L, Baldinger S, Hag-alshiekh M, Bostrom B, Sencer S, D'Andrea AD. Hirsch B, et al. Blood. 2004 Apr 1;103(7):2554-9. doi: 10.1182/blood-2003-06-1970. Epub 2003 Dec 11. Blood. 2004. PMID: 14670928 Free article.

2

Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2).

McReynolds LJ, Biswas K, Giri N, Sharan SK, Alter BP. McReynolds LJ, et al. Cancer Genet. 2021 Nov;258-259:101-109. doi: 10.1016/j.cancergen.2021.10.001. Epub 2021 Oct 4. Cancer Genet. 2021. PMID: 34687993 Free PMC article.

3

The clinical phenotype of children with Fanconi anemia caused by biallelic FANCD1/BRCA2 mutations.

Myers K, Davies SM, Harris RE, Spunt SL, Smolarek T, Zimmerman S, McMasters R, Wagner L, Mueller R, Auerbach AD, Mehta PA. Myers K, et al. Pediatr Blood Cancer. 2012 Mar;58(3):462-5. doi: 10.1002/pbc.23168. Epub 2011 May 5. Pediatr Blood Cancer. 2012. PMID: 21548014

4

[Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report].

Puchmajerová A, Švojgr K, Novotná D, Macháčková E, Sumerauer D, Smíšek P, Kodet R, Kynčl M, Křepelová A, Foretová L. Puchmajerová A, et al. Klin Onkol. 2016;29 Suppl 1:S89-92. doi: 10.14735/amko2016s89. Klin Onkol. 2016. PMID: 26691948 Czech.

5

Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour.

Reid S, Renwick A, Seal S, Baskcomb L, Barfoot R, Jayatilake H, Pritchard-Jones K, Stratton MR, Ridolfi-Lüthy A, Rahman N; Breast Cancer Susceptibility Collaboration (UK); Familial Wilms Tumour Collaboration. Reid S, et al. J Med Genet. 2005 Feb;42(2):147-51. doi: 10.1136/jmg.2004.022673. J Med Genet. 2005. PMID: 15689453 Free PMC article. No abstract available.

6

Fanconi anemia and solid malignancies in childhood: a national retrospective study.

Malric A, Defachelles AS, Leblanc T, Lescoeur B, Lacour B, Peuchmaur M, Maurage CA, Pierron G, Guillemot D, d'Enghien CD, Soulier J, Stoppa-Lyonnet D, Bourdeaut F. Malric A, et al. Pediatr Blood Cancer. 2015 Mar;62(3):463-70. doi: 10.1002/pbc.25303. Epub 2014 Nov 8. Pediatr Blood Cancer. 2015. PMID: 25381700 Clinical Trial.

7

Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia.

Offit K, Levran O, Mullaney B, Mah K, Nafa K, Batish SD, Diotti R, Schneider H, Deffenbaugh A, Scholl T, Proud VK, Robson M, Norton L, Ellis N, Hanenberg H, Auerbach AD. Offit K, et al. J Natl Cancer Inst. 2003 Oct 15;95(20):1548-51. doi: 10.1093/jnci/djg072. J Natl Cancer Inst. 2003. PMID: 14559878

8

Fanconi anemia and biallelic BRCA2 mutation diagnosed in a young child with an embryonal CNS tumor.

Dewire MD, Ellison DW, Patay Z, McKinnon PJ, Sanders RP, Gajjar A. Dewire MD, et al. Pediatr Blood Cancer. 2009 Dec;53(6):1140-2. doi: 10.1002/pbc.22139. Pediatr Blood Cancer. 2009. PMID: 19530235 Free PMC article.

9

Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.

Feben C, Spencer C, Lochan A, Laing N, Fieggen K, Honey E, Wainstein T, Krause A. Feben C, et al. Fam Cancer. 2017 Jul;16(3):441-446. doi: 10.1007/s10689-017-9968-y. Fam Cancer. 2017. PMID: 28185119

10

Fanconi anemia gene mutations are not involved in sporadic Wilms tumor.

Adank MA, Segers H, van Mil SE, van Helsdingen YM, Ameziane N, van den Ouweland AM, Wagner A, Meijers-Heijboer H, Kool M, de Kraker J, Waisfisz Q, van den Heuvel-Eibrink MM. Adank MA, et al. Pediatr Blood Cancer. 2010 Oct;55(4):742-4. doi: 10.1002/pbc.22588. Pediatr Blood Cancer. 2010. PMID: 20589654

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