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Items: 1 to 20 of 43

1.

Hexasomy 13q31.3q34 due to two marker chromosomes with inverted duplication in a fetus with increased nuchal translucency.

Stembalska A, Jagielska G, Laczmanska I, Szmida E, Jarczynska A, Gil J.

Birth Defects Res A Clin Mol Teratol. 2015 Apr;103(4):255-9. doi: 10.1002/bdra.23344. Epub 2015 Apr 7.

PMID:
25852029
2.

Origin of a prenatal mosaic supernumerary neocentromeric derivative chromosome 13 determined by QF-PCR.

Dawson AJ, Hryshko M, Konkin D, Bal S, Bernier D, Tomiuk M, Burnett S, Frosk P, Chodirker BN, Chun K.

Fetal Diagn Ther. 2013;33(1):75-8. doi: 10.1159/000337537. Epub 2012 May 17.

PMID:
22614064
3.

Silencing of unpaired meiotic chromosomes and altered recombination patterns in an azoospermic carrier of a t(8;13) reciprocal translocation.

Ferguson KA, Chow V, Ma S.

Hum Reprod. 2008 Apr;23(4):988-95. doi: 10.1093/humrep/den013. Epub 2008 Feb 12.

PMID:
18270180
4.

Synergistic action of the microRNA-17 polycistron and Myc in aggressive cancer development.

Tagawa H, Karube K, Tsuzuki S, Ohshima K, Seto M.

Cancer Sci. 2007 Sep;98(9):1482-90. Epub 2007 Jun 30. Erratum in: Cancer Sci. 2008 Jan;99(1):186.

5.

Constitutional complex chromosomal rearrangements in azoospermic men--case report and literature review.

Lee IW, Su MT, Hsu CC, Lin YH, Chen PY, Kuo PL.

Urology. 2006 Dec;68(6):1343.e5-8.

PMID:
17169659
6.

Hydrocephaly, penoscrotal transposition, and digital anomalies associated with de novo pseudodicentric rearranged chromosome 13 characterized by classical cytogenetic methods and mBAND analysis.

Christofolini DM, Yoshimoto M, Squire JA, Brunoni D, Melaragno MI, Carvalheira G.

Am J Med Genet A. 2006 Jun 15;140(12):1321-5.

PMID:
16691582
7.

Neoplastic circulating endothelial cells in multiple myeloma with 13q14 deletion.

Rigolin GM, Fraulini C, Ciccone M, Mauro E, Bugli AM, De Angeli C, Negrini M, Cuneo A, Castoldi G.

Blood. 2006 Mar 15;107(6):2531-5. Epub 2005 Nov 29.

8.

Characterization of a familial balanced rec(13) in a child with mild MR and his half-sibling with two structurally rearranged chromosomes 13.

Mehra S, Christ L, Jeng L, Zinn AB, Schwartz S.

Am J Med Genet A. 2005 Aug 30;137(2):217-21. Review.

PMID:
16059944
9.

The DNA sequence and analysis of human chromosome 13.

Dunham A, Matthews LH, Burton J, Ashurst JL, Howe KL, Ashcroft KJ, Beare DM, Burford DC, Hunt SE, Griffiths-Jones S, Jones MC, Keenan SJ, Oliver K, Scott CE, Ainscough R, Almeida JP, Ambrose KD, Andrews DT, Ashwell RI, Babbage AK, Bagguley CL, Bailey J, Bannerjee R, Barlow KF, Bates K, Beasley H, Bird CP, Bray-Allen S, Brown AJ, Brown JY, Burrill W, Carder C, Carter NP, Chapman JC, Clamp ME, Clark SY, Clarke G, Clee CM, Clegg SC, Cobley V, Collins JE, Corby N, Coville GJ, Deloukas P, Dhami P, Dunham I, Dunn M, Earthrowl ME, Ellington AG, Faulkner L, Frankish AG, Frankland J, French L, Garner P, Garnett J, Gilbert JG, Gilson CJ, Ghori J, Grafham DV, Gribble SM, Griffiths C, Hall RE, Hammond S, Harley JL, Hart EA, Heath PD, Howden PJ, Huckle EJ, Hunt PJ, Hunt AR, Johnson C, Johnson D, Kay M, Kimberley AM, King A, Laird GK, Langford CJ, Lawlor S, Leongamornlert DA, Lloyd DM, Lloyd C, Loveland JE, Lovell J, Martin S, Mashreghi-Mohammadi M, McLaren SJ, McMurray A, Milne S, Moore MJ, Nickerson T, Palmer SA, Pearce AV, Peck AI, Pelan S, Phillimore B, Porter KM, Rice CM, Searle S, Sehra HK, Shownkeen R, Skuce CD, Smith M, Steward CA, Sycamore N, Tester J, Thomas DW, Tracey A, Tromans A, Tubby B, Wall M, Wallis JM, West AP, Whitehead SL, Willey DL, Wilming L, Wray PW, Wright MW, Young L, Coulson A, Durbin R, Hubbard T, Sulston JE, Beck S, Bentley DR, Rogers J, Ross MT.

Nature. 2004 Apr 1;428(6982):522-8.

10.

Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres.

Alonso A, Mahmood R, Li S, Cheung F, Yoda K, Warburton PE.

Hum Mol Genet. 2003 Oct 15;12(20):2711-21. Epub 2003 Aug 19.

PMID:
12928482
11.

A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities.

Cockwell AE, Jacobs PA, Beal SJ, Crolla JA.

Hum Genet. 2003 Mar;112(3):298-302. Epub 2003 Jan 8.

PMID:
12596054
12.

Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies.

Alves C, Carvalho F, Cremades N, Sousa M, Barros A.

Eur J Hum Genet. 2002 Aug;10(8):467-74.

13.

A new translocation t(11;13)(q13;q14) in a mature B-cell neoplasm.

Solé F, Salido M, Espinet B, Zamora L, Berlanga J, Domingo A.

Haematologica. 2002 Jul;87(7):777-8.

14.

First case of trisomy 13 plus mosaic trisomy 1q.

Liehr T, Schmidt M, Starke H, Ziegler M, Kittner G, Heller A, Rubtsov N, Trifonov V, Claussen U.

Fetal Diagn Ther. 2002 May-Jun;17(3):133-6.

PMID:
11914563
15.

Establishment of the B cell precursor acute lymphoblastic leukemia cell line MUTZ-5 carrying a (12:13) translocation.

Meyer C, MacLeod RA, Quentmeier H, Janssen JW, Coignet LJ, Dyer MJ, Drexler HG.

Leukemia. 2001 Sep;15(9):1471-4.

PMID:
11516110
16.

[Evolutionarily-conserved gene CKAP2,located in region 13q14.3 of the human genome, is frequently rearranged in various tumors].

Udina IG, Baranova AV, Kompaniń≠tsev AA, Sulimova GE.

Genetika. 2001 Jan;37(1):120-3. Russian.

PMID:
11234418
17.

Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.

Warburton PE, Dolled M, Mahmood R, Alonso A, Li S, Naritomi K, Tohma T, Nagai T, Hasegawa T, Ohashi H, Govaerts LC, Eussen BH, Van Hemel JO, Lozzio C, Schwartz S, Dowhanick-Morrissette JJ, Spinner NB, Rivera H, Crolla JA, Yu C, Warburton D.

Am J Hum Genet. 2000 Jun;66(6):1794-806. Epub 2000 Apr 24. Review.

18.

Translocation (8;13)(q24.2;q33) in a malignant rhabdoid tumor of the liver.

Donner LR, Rao A, Truss LM, Dobin SM.

Cancer Genet Cytogenet. 2000 Jan 15;116(2):153-7.

PMID:
10640148
19.

Physical assignments of human chromosome 13 genes on pig chromosome 11 demonstrate extensive synteny and gene order conservation between pig and human.

Sun HS, Yerle M, Pinton P, Chardon P, Rogel-Gaillard C, Lyons LA, Laughlin TF, Tuggle CK.

Anim Genet. 1999 Aug;30(4):304-8.

PMID:
10467706
20.

HMG1 is not rearranged by 13q12 aberrations in lipomas.

Kazmierczak B, Dal Cin P, Meyer-Bolte K, Van den Berghe H, Bullerdiek J.

Genes Chromosomes Cancer. 1999 Mar;24(3):290-2.

PMID:
10451712

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