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Select item 229437241.

Detection of identical unbalanced karyotype in two consequent fetuses due to a maternal pericentric inversion of chromosome 18.

Sahin FI, Ozer O, Tarim E, Yilmaz Z.

J Obstet Gynaecol. 2012 Oct;32(7):698-700. doi: 10.3109/01443615.2012.702151. No abstract available.

PMID:: 22943724; [PubMed - indexed for MEDLINE]

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Select item 215679092.

Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q.

Breman AM, Probst FJ, Blazo MA, Schaaf CP, Roney EK, Craigen WJ, Bacino CA, Cheung SW.

Am J Med Genet A. 2011 Jun;155A(6):1465-8. doi: 10.1002/ajmg.a.33935. Epub 2011 May 12. No abstract available.

PMID:: 21567909; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 215633123.

Gene-centric view on the human proteome project: the example of the Russian roadmap for chromosome 18.

Archakov A, Aseev A, Bykov V, Grigoriev A, Govorun V, Ivanov V, Khlunov A, Lisitsa A, Mazurenko S, Makarov AA, Ponomarenko E, Sagdeev R, Skryabin K.

Proteomics. 2011 May;11(10):1853-6. doi: 10.1002/pmic.201000540.

PMID:: 21563312; [PubMed - indexed for MEDLINE]

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Select item 214767934.

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; [PubMed - indexed for MEDLINE]

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Select item 213337645.

De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems.

Lo-Castro A, El-Malhany N, Galasso C, Verrotti A, Nardone AM, Postorivo D, Palmieri C, Curatolo P.

Eur J Med Genet. 2011 May-Jun;54(3):329-32. doi: 10.1016/j.ejmg.2011.02.004. Epub 2011 Feb 17.

PMID:: 21333764; [PubMed - indexed for MEDLINE]

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Select item 213262866.

Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18.

Kariminejad A, Kariminejad R, Moshtagh A, Zanganeh M, Kariminejad MH, Neuenschwander S, Okoniewski M, Wey E, Schinzel A, Baumer A.

Eur J Hum Genet. 2011 May;19(5):555-60. doi: 10.1038/ejhg.2010.252. Epub 2011 Feb 16.

PMID:: 21326286; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 211047847.

Common pathogenetic mechanism involving human chromosome 18 in familial and sporadic ileal carcinoid tumors.

Cunningham JL, Díaz de Ståhl T, Sjöblom T, Westin G, Dumanski JP, Janson ET.

Genes Chromosomes Cancer. 2011 Feb;50(2):82-94. doi: 10.1002/gcc.20834.

PMID:: 21104784; [PubMed - indexed for MEDLINE]

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Select item 210608958.

Identification of candidate genes for dyslexia susceptibility on chromosome 18.

Scerri TS, Paracchini S, Morris A, MacPhie IL, Talcott J, Stein J, Smith SD, Pennington BF, Olson RK, DeFries JC, Monaco AP, Richardson AJ.

PLoS One. 2010 Oct 28;5(10):e13712. doi: 10.1371/journal.pone.0013712. Erratum in: PLoS One. 2010;5(12). doi: 10.1371/annotation/2294a38b-878d-42f0-9faf-0822db4a0248. Richardson, Alex J [added].

PMID:: 21060895; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 208647869.

Prenatal diagnosis and molecular cytogenetic analysis of a de novo isodicentric chromosome 18.

Zhang Y, Dai Y, Ren J, Wang L.

Ann Saudi Med. 2010 Nov-Dec;30(6):489-92.

PMID:: 20864786; [PubMed - indexed for MEDLINE]

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Select item 2070852610.

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18.

Chen CP, Lin CC, Su YN, Tsai FJ, Chen JT, Chern SR, Lee CC, Town DD, Chen LF, Wu PC, Wang W.

Taiwan J Obstet Gynecol. 2010 Jun;49(2):188-91. doi: 10.1016/S1028-4559(10)60039-3.

PMID:: 20708526; [PubMed - indexed for MEDLINE]

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Select item 2066189611.

Locus-specific dual color-probe for the enumeration of chromosome 18 in rapid FISH aneuploidy testing on uncultured amniocytes.

Soucy JF, Lavoie J, Duncan AM.

Prenat Diagn. 2010 Aug;30(8):811-2. doi: 10.1002/pd.2569. No abstract available.

PMID:: 20661896; [PubMed - indexed for MEDLINE]

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Select item 2064998412.

Ring chromosome 18 abnormality in acute myelogenous leukemia: the clinical dilemma.

Sivendran S, Gruenstein S, Malone AK, Najfeld V.

J Hematol Oncol. 2010 Jul 22;3:25. doi: 10.1186/1756-8722-3-25.

PMID:: 20649984; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 2042003513.

Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q).

Prontera P, Buldrini B, Aiello V, Rogaia D, Mencarelli A, Gruppioni R, Bonfatti A, Beltrami N, Donti E, Sensi A.

Genet Couns. 2010;21(1):91-7.

PMID:: 20420035; [PubMed - indexed for MEDLINE]

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Select item 1992730714.

Psychiatric syndromes in individuals with chromosome 18 abnormalities.

Zavala J, Ramirez M, Medina R, Heard P, Carter E, Crandall A, Hale D, Cody J, Escamilla M.

Am J Med Genet B Neuropsychiatr Genet. 2010 Apr 5;153B(3):837-45. doi: 10.1002/ajmg.b.31047.

PMID:: 19927307; [PubMed - indexed for MEDLINE]

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Select item 1991141415.

False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite probe (D18Z1) to chromosome 2.

Collin A, Sladkevicius P, Soller M.

Prenat Diagn. 2009 Dec;29(13):1279-81. doi: 10.1002/pd.2401. No abstract available.

PMID:: 19911414; [PubMed - indexed for MEDLINE]

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Select item 1981688016.

Fluorescence in situ hybridization in prenatal screening: lessons from an inherited chromosome 18 marker.

Valentin M, Ottenwalter A, Serero S, Muller F, Luton D, Ducarme G.

Prenat Diagn. 2009 Dec;29(12):1177-9. doi: 10.1002/pd.2381. No abstract available.

PMID:: 19816880; [PubMed - indexed for MEDLINE]

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Select item 1974574717.

A gene dosage map of Chromosome 18: a map with clinical utility.

Cody JD, Carter EM, Sebold C, Heard PL, Hale DE.

Genet Med. 2009 Nov;11(11):778-82. doi: 10.1097/GIM.0b013e3181b6573d.

PMID:: 19745747; [PubMed - indexed for MEDLINE]

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Select item 1969089018.

Genetic analysis of diabetic nephropathy on chromosome 18 in African Americans: linkage analysis and dense SNP mapping.

McDonough CW, Bostrom MA, Lu L, Hicks PJ, Langefeld CD, Divers J, Mychaleckyj JC, Freedman BI, Bowden DW.

Hum Genet. 2009 Dec;126(6):805-17. doi: 10.1007/s00439-009-0732-8.

PMID:: 19690890; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 1950080119.

Prognostic role of loss of heterozygosity on chromosome 18 in patients with low-risk nonmuscle-invasive bladder cancer: results from a prospective study.

Cai T, Nesi G, Dal Canto M, Mondaini N, Piazzini M, Bartoletti R.

J Surg Res. 2010 Jun 1;161(1):89-94. doi: 10.1016/j.jss.2008.10.017. Epub 2008 Nov 21.

PMID:: 19500801; [PubMed - indexed for MEDLINE]

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Select item 1949573920.

Spatial allelic imbalance of BCL2 genes and chromosome 18 territories in nonneoplastic and neoplastic cervical squamous epithelium.

Wiech T, Stein S, Lachenmaier V, Schmitt E, Schwarz-Finsterle J, Wiech E, Hildenbrand G, Werner M, Hausmann M.

Eur Biophys J. 2009 Jul;38(6):793-806. doi: 10.1007/s00249-009-0474-5. Epub 2009 Jun 3.

PMID:: 19495739; [PubMed - indexed for MEDLINE]

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7 free full-text articles in PubMed Central

Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q. [Am J Med Genet A. 2011]
Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q.
Breman AM, Probst FJ, Blazo MA, Schaaf CP, Roney EK, Craigen WJ, Bacino CA, Cheung SW. Am J Med Genet A. 2011 Jun; 155A(6):1465-8. Epub 2011 May 12.
Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18. [Eur J Hum Genet. 2011]
Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18.
Kariminejad A, Kariminejad R, Moshtagh A, Zanganeh M, Kariminejad MH, Neuenschwander S, Okoniewski M, Wey E, Schinzel A, Baumer A. Eur J Hum Genet. 2011 May; 19(5):555-60. Epub 2011 Feb 16.
Identification of candidate genes for dyslexia susceptibility on chromosome 18. [PLoS One. 2010]
Identification of candidate genes for dyslexia susceptibility on chromosome 18.
Scerri TS, Paracchini S, Morris A, MacPhie IL, Talcott J, Stein J, Smith SD, Pennington BF, Olson RK, DeFries JC, et al. PLoS One. 2010 Oct 28; 5(10):e13712. Epub 2010 Oct 28.

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