Similar articles for PMID: 19644022

Year	Number of Results
1994	1
1995	1
1997	1
1998	2
1999	9
2000	9
2001	5
2002	2
2003	7
2004	7
2005	8
2006	8
2007	8
2008	4
2009	9
2010	5
2012	5
2013	2
2014	4
2015	1
2016	1
2017	1
2020	2
2022	1
2023	1
2024	0

1

Evaluation of 13q14 status in multiple myeloma by digital single nucleotide polymorphism technology.

Hanlon K, Harries LW, Ellard S, Rudin CE. Hanlon K, et al. J Mol Diagn. 2009 Sep;11(5):450-7. doi: 10.2353/jmoldx.2009.090027. Epub 2009 Jul 30. J Mol Diagn. 2009. PMID: 19644022 Free PMC article.

2

Evaluation of 13q14 status in patients with chronic lymphocytic leukemia using single nucleotide polymorphism-based techniques.

Hanlon K, Ellard S, Rudin CE, Thorne S, Davies T, Harries LW. Hanlon K, et al. J Mol Diagn. 2009 Jul;11(4):298-305. doi: 10.2353/jmoldx.2009.080167. Epub 2009 May 21. J Mol Diagn. 2009. PMID: 19460942 Free PMC article.

3

Interstitial deletions at the long arm of chromosome 13 may be as common as monosomies in multiple myeloma. A genotypic study.

Nomdedéu JF, Lasa A, Ubeda J, Saglio G, Bellido M, Casas S, Carnicer MJ, Aventín A, Sureda A, Sierra J, Baiget M. Nomdedéu JF, et al. Haematologica. 2002 Aug;87(8):828-35. Haematologica. 2002. PMID: 12161359

4

Deletions of chromosome 13 in multiple myeloma identified by interphase FISH usually denote large deletions of the q arm or monosomy.

Fonseca R, Oken MM, Harrington D, Bailey RJ, Van Wier SA, Henderson KJ, Kay NE, Van Ness B, Greipp PR, Dewald GW. Fonseca R, et al. Leukemia. 2001 Jun;15(6):981-6. doi: 10.1038/sj.leu.2402125. Leukemia. 2001. PMID: 11417487 Clinical Trial.

5

Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes.

Svobodova K, Zemanova Z, Lhotska H, Novakova M, Podskalska L, Belickova M, Brezinova J, Sarova I, Izakova S, Lizcova L, Berkova A, Siskova M, Jonasova A, Cermak J, Michalova K. Svobodova K, et al. Leuk Res. 2016 Mar;42:7-12. doi: 10.1016/j.leukres.2016.01.009. Epub 2016 Jan 24. Leuk Res. 2016. PMID: 26851439

6

Analysis for loss of heterozygosity on chromosome arm 13q by STR analysis or SNP sequencing can replace analysis of FLT3-ITD to detect patients with prognostically adverse AML.

Schnittger S, Haferlach C, Kern W, Haferlach T. Schnittger S, et al. Genes Chromosomes Cancer. 2014 Dec;53(12):1008-17. doi: 10.1002/gcc.22210. Epub 2014 Sep 3. Genes Chromosomes Cancer. 2014. PMID: 25183446

7

Use of plasma DNA in detection of loss of heterozygosity in patients with multiple myeloma.

Ahmed M, Giles F, Joe Y, Weber DM, Jilani I, Manshouri T, Giralt S, De Lima M, Keating M, Albitar M. Ahmed M, et al. Eur J Haematol. 2003 Sep;71(3):174-8. doi: 10.1034/j.1600-0609.2003.00125.x. Eur J Haematol. 2003. PMID: 12930317

8

Consistent patterns of allelic loss in natural killer cell lymphoma.

Siu LL, Chan V, Chan JK, Wong KF, Liang R, Kwong YL. Siu LL, et al. Am J Pathol. 2000 Dec;157(6):1803-9. doi: 10.1016/S0002-9440(10)64818-3. Am J Pathol. 2000. PMID: 11106552 Free PMC article.

9

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers.

Gaasenbeek M, Howarth K, Rowan AJ, Gorman PA, Jones A, Chaplin T, Liu Y, Bicknell D, Davison EJ, Fiegler H, Carter NP, Roylance RR, Tomlinson IP. Gaasenbeek M, et al. Cancer Res. 2006 Apr 1;66(7):3471-9. doi: 10.1158/0008-5472.CAN-05-3285. Cancer Res. 2006. PMID: 16585170

10

Molecular cytogenetic aberrations in patients with multiple myeloma studied by interphase fluorescence in situ hybridization.

Chen L, Li J, Xu W, Qiu H, Zhu Y, Zhang Y, Duan L, Qian S, Lu H. Chen L, et al. Exp Oncol. 2007 Jun;29(2):116-20. Exp Oncol. 2007. PMID: 17704743

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