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Results: 1 to 20 of 121

Similar articles for PubMed (Select 24729308)

1.

Confined trisomy 8 mosaicism of meiotic origin: a rare cause of aneuploidy in childhood cancer.

Valind A, Pal N, Asmundsson J, Gisselsson D, Holmquist Mengelbier L.

Genes Chromosomes Cancer. 2014 Jul;53(7):634-8. doi: 10.1002/gcc.22173. Epub 2014 Apr 12.

PMID:
24729308
2.

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.

Conlin LK, Thiel BD, Bonnemann CG, Medne L, Ernst LM, Zackai EH, Deardorff MA, Krantz ID, Hakonarson H, Spinner NB.

Hum Mol Genet. 2010 Apr 1;19(7):1263-75. doi: 10.1093/hmg/ddq003. Epub 2010 Jan 6.

3.

Partial trisomy 8 mosaicism due to a pseudoisodicentric chromosome 8.

Leon E, Jamal SM, Zou YS, Milunsky JM.

Am J Med Genet A. 2011 Jul;155A(7):1740-4. doi: 10.1002/ajmg.a.34073. Epub 2011 Jun 10.

PMID:
21671393
4.

Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies.

Ensenauer RE, Shaughnessy WJ, Jalal SM, Dawson DB, Courteau LK, Ellison JW.

Am J Med Genet A. 2005 Apr 15;134A(2):202-6. Review.

PMID:
15690403
5.

Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia.

Minelli A, Morerio C, Maserati E, Olivieri C, Panarello C, Bonvini L, Leszl A, Rosanda C, Lanino E, Danesino C, Pasquali F.

Leukemia. 2001 Jun;15(6):971-5.

PMID:
11417485
6.

Constitutional partial 1q trisomy mosaicism and Wilms tumor.

Mark HF, Wyandt H, Pan A, Milunsky JM.

Cancer Genet Cytogenet. 2005 Oct 15;162(2):166-71.

PMID:
16213366
7.

Pre- and postnatal findings in trisomy 17 mosaicism.

Utermann B, Riegel M, Leistritz D, Karall T, Wisser J, Meisner L, Fauth C, Baldinger R, Johnson J, Erdel M, Taralczak M, Pauli RM, Baumer A, Schinzel A, Kotzot D.

Am J Med Genet A. 2006 Aug 1;140(15):1628-36.

PMID:
16802327
8.

Double autosomal/gonosomal mosaic aneuploidy: study of nondisjunction in two cases with trisomy of chromosome 8.

DeBrasi D, Genardi M, D'Agostino A, Calvieri F, Tozzi C, Varrone S, Neri G.

Hum Genet. 1995 May;95(5):519-25.

PMID:
7759072
9.

Hyperdiploidy including trisomy 8 in a cystic partially differentiated nephroblastoma.

Timmons CF, McGavran L, Unterkircher L, Beckwith JB, Wilson HL.

Cancer Genet Cytogenet. 1989 Aug;41(1):79-85.

PMID:
2548706
10.

Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.

Genuardi M, Tozzi C, Pomponi MG, Stagni ML, Della Monica M, Scarano G, Calvieri F, Torrisi L, Neri G.

Eur J Hum Genet. 1999 May-Jun;7(4):421-6.

11.

Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndrome.

Petit F, Holder-Espinasse M, Duban-Bedu B, Bouquillon S, Boute-Benejean O, Bazin A, Rouland V, Manouvrier-Hanu S, Delobel B.

Clin Genet. 2012 Mar;81(3):265-71. doi: 10.1111/j.1399-0004.2010.01621.x. Epub 2011 Jan 19.

PMID:
21204802
12.

Whole chromosome gain does not in itself confer cancer-like chromosomal instability.

Valind A, Jin Y, Baldetorp B, Gisselsson D.

Proc Natl Acad Sci U S A. 2013 Dec 24;110(52):21119-23. doi: 10.1073/pnas.1311163110. Epub 2013 Dec 9.

13.

Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.

Schinzel A, Kotzot D, Brecevic L, Robinson WP, Dutly F, Dauwerse H, Binkert F, Baumer A, Ausserer B.

Eur J Hum Genet. 1997 Sep-Oct;5(5):308-14.

PMID:
9412788
14.

Two unique patients with trisomy 18 mosaicism and molecular marker studies.

Slavotinek A, Poyser L, Wallace A, Martin F, Gaunt L, Kingston H.

Am J Med Genet A. 2003 Mar 15;117A(3):282-8.

PMID:
12599194
15.

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction.

Robinson WP, Barrett IJ, Bernard L, Telenius A, Bernasconi F, Wilson RD, Best RG, Howard-Peebles PN, Langlois S, Kalousek DK.

Am J Hum Genet. 1997 Apr;60(4):917-27.

16.

[Detection of mosaic trisomy 9 missed by conventional cytogenetics using SNP-array and fluorescence in situ hybridization].

Luo Y, Chen S, Li H, Pan L, Shen M, Jin F, Xu C.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):469-71. doi: 10.3760/cma.j.issn.1003-9406.2014.04.012. Chinese.

PMID:
25119912
17.

Mosaic double aneuploidy (45,X/47,XX,+8) with aortic dissection.

Lee MN, Choi KH, Kim DK, Kim SH.

Genet Couns. 2014;25(2):177-82.

PMID:
25059016
18.

Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line.

Bruyère H, Rupps R, Kuchinka BD, Friedman JM, Robinson WP.

Am J Med Genet. 2000 Sep 4;94(1):35-41.

PMID:
10982480
19.

Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.

Grati FR, Grimi B, Frascoli G, Di Meco AM, Liuti R, Milani S, Trotta A, Dulcetti F, Grosso E, Miozzo M, Maggi F, Simoni G.

Eur J Hum Genet. 2006 Mar;14(3):282-8.

20.

Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism.

Chen CP, Huang HK, Su YN, Chern SR, Su JW, Lee CC, Town DD, Chen WL, Chen YT, Wang W.

Taiwan J Obstet Gynecol. 2012 Mar;51(1):77-82. doi: 10.1016/j.tjog.2012.01.015.

PMID:
22482973
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