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Items: 18

1.

Supernumerary marker chromosomes derived from chromosome 6: cytogenetic, molecular cytogenetic, and array CGH characterization.

Huang B, Pearle P, Rauen KA, Cotter PD.

Am J Med Genet A. 2012 Jul;158A(7):1568-73. doi: 10.1002/ajmg.a.35385. Epub 2012 May 25.

2.

A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity.

Reddy KS, Aradhya S, Meck J, Tiller G, Abboy S, Bass H.

Genet Med. 2013 Jan;15(1):3-13. doi: 10.1038/gim.2012.78. Epub 2012 Aug 30. Review.

PMID:
22935720
3.
4.

Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes.

Liehr T, Klein E, Mrasek K, Kosyakova N, Guilherme RS, Aust N, Venner C, Weise A, Hamid AB.

Cytogenet Genome Res. 2013;139(3):158-63. doi: 10.1159/000346026. Epub 2012 Dec 29. Review.

PMID:
23295254
5.

[Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics].

Douet-Guilbert N, Basinko A, Le Bris MJ, Herry A, Morel F, De Braekeleer M.

Pathol Biol (Paris). 2008 Sep;56(6):362-7. doi: 10.1016/j.patbio.2008.03.012. Epub 2008 May 5. Review. French.

PMID:
18456432
6.

Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.

Chen CP, Lin CC, Li YC, Chern SR, Lee CC, Chen WL, Lee MS, Wang W, Tzen CY.

Prenat Diagn. 2004 Oct;24(10):767-73. Review.

PMID:
15503270
7.

Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications.

Yatsenko SA, Treadwell-Deering D, Krull K, Lewis RA, Glaze D, Stankiewicz P, Lupski JR, Potocki L.

Am J Med Genet A. 2005 Oct 1;138A(2):175-80. Review.

PMID:
16152635
8.

Cytogenomic and phenotypic analysis in low-level monosomy 7 mosaicism with non-supernumerary ring chromosome 7.

Salas-Labadía C, Cervantes-Barragán DE, Cruz-Alcívar R, Daber RD, Conlin LK, Leonard LD, Spinner NB, Durán-McKinster C, Dávila-Ortíz de Montellano DJ, Del Castillo-Ruiz V, Pérez-Vera P.

Am J Med Genet A. 2014 Jul;164A(7):1765-9. doi: 10.1002/ajmg.a.36503. Epub 2014 Mar 26. Review.

PMID:
24677512
10.

Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8.

Starke H, Schreyer I, Kähler C, Fiedler W, Beensen V, Heller A, Nietzel A, Claussen U, Liehr T.

Prenat Diagn. 1999 Dec;19(12):1169-74. Review.

PMID:
10590438
11.

De-novo 'pure' partial trisomy (6)(p22.3→pter): a case report and review of the literature.

Sivasankaran A, Murthy K, Oruganti VP, Deenadayalu A, R Samuel C, Kandukuri LR.

Clin Dysmorphol. 2017 Jan;26(1):26-32. Review.

PMID:
27759572
12.
13.

Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.

Melo JB, Backx L, Vermeesch JR, Santos HG, Sousa AC, Kosyakova N, Weise A, von Eggeling F, Liehr T, Carreira IM.

J Appl Genet. 2011 May;52(2):193-200. doi: 10.1007/s13353-011-0035-3. Epub 2011 Mar 25. Review.

PMID:
21437654
14.

[Advances in rapid prenatal detection of fetal chromosome abnormalities].

Wang J, Cui YX.

Zhonghua Nan Ke Xue. 2010 Apr;16(4):359-63. Review. Chinese.

PMID:
20626168
15.

Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature.

Evangelidou P, Alexandrou A, Moutafi M, Ioannides M, Antoniou P, Koumbaris G, Kallikas I, Velissariou V, Sismani C, Patsalis PC.

Biomed Res Int. 2013;2013:346762. doi: 10.1155/2013/346762. Epub 2013 Mar 4. Review.

16.

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.

Liehr T, Starke H, Senger G, Melotte C, Weise A, Vermeesch JR.

Am J Med Genet A. 2006 Jan 1;140(1):46-51. Review.

PMID:
16333826
17.

Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18--how to counsel?

Eckmann-Scholz C, Tönnies H, Liehr T, Gesk S, Jonat W, Caliebe A.

J Matern Fetal Neonatal Med. 2012 Feb;25(2):200-2. doi: 10.3109/14767058.2011.566949. Epub 2011 Apr 8. Review.

PMID:
21476793
18.

Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16.

Hengstschläger M, Bettelheim D, Drahonsky R, Deutinger J, Bernaschek G.

Prenat Diagn. 2001 Jun;21(6):477-80. Review.

PMID:
11438953

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