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Results: 16

Select item 234032381.

Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.

Chen CP, Lin CJ, Chang TY, Chern SR, Wu PS, Chen YT, Su JW, Lee CC, Chen LF, Wang W.

Gene. 2013 Apr 25;519(1):164-8. doi: 10.1016/j.gene.2013.01.055. Epub 2013 Feb 9.

PMID:: 23403238; [PubMed - indexed for MEDLINE]

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Select item 230409272.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.

Chen CP, Chen M, Chern SR, Wu PS, Chang SP, Lee DJ, Chen YT, Chen LF, Su JW, Hwa-Ruey Hsieh A, Hwa-Jiun Hsieh A, Wang W.

Taiwan J Obstet Gynecol. 2012 Sep;51(3):411-7. doi: 10.1016/j.tjog.2012.07.017.

PMID:: 23040927; [PubMed - indexed for MEDLINE]

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Select item 228216803.

Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutation in AGXT and a terminal deletion of chromosome 2.

Tammachote R, Kingsuwannapong N, Tongkobpetch S, Srichomthong C, Yeetong P, Kingwatanakul P, Monico CG, Suphapeetiporn K, Shotelersuk V.

Am J Med Genet A. 2012 Sep;158A(9):2124-30. doi: 10.1002/ajmg.a.35495. Epub 2012 Jul 20.

PMID:: 22821680; [PubMed - indexed for MEDLINE]

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Select item 224191674.

The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2.

Ventura M, Catacchio CR, Sajjadian S, Vives L, Sudmant PH, Marques-Bonet T, Graves TA, Wilson RK, Eichler EE.

Genome Res. 2012 Jun;22(6):1036-49. doi: 10.1101/gr.136556.111. Epub 2012 Mar 14.

PMID:: 22419167; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 221234905.

Coamplification of multiple regions of chromosome 2, including MYCN, in a single patchwork amplicon in cancer cell lines.

Kitada K, Aida S, Aikawa S.

Cytogenet Genome Res. 2012;136(1):30-7. doi: 10.1159/000334349. Epub 2011 Nov 23.

PMID:: 22123490; [PubMed - indexed for MEDLINE]

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Select item 213856586.

De novo interstitial deletion of chromosome 2 (p23p24).

Su PH, Chen JY, Tsao TF, Chen SJ.

Pediatr Neonatol. 2011 Feb;52(1):46-50. doi: 10.1016/j.pedneo.2010.12.001. Epub 2011 Feb 18.

PMID:: 21385658; [PubMed - indexed for MEDLINE]

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Select item 206840157.

Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism.

Devillard F, Guinchat V, Moreno-De-Luca D, Tabet AC, Gruchy N, Guillem P, Nguyen Morel MA, Leporrier N, Leboyer M, Jouk PS, Lespinasse J, Betancur C.

Am J Med Genet A. 2010 Sep;152A(9):2346-54. doi: 10.1002/ajmg.a.33601.

PMID:: 20684015; [PubMed - indexed for MEDLINE]

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Select item 205831748.

Paternal isodisomy of chromosome 2 as a cause of long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency.

Baskin B, Geraghty M, Ray PN.

Am J Med Genet A. 2010 Jul;152A(7):1808-11. doi: 10.1002/ajmg.a.33462.

PMID:: 20583174; [PubMed - indexed for MEDLINE]

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Select item 204680719.

Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts.

Dick DM, Meyers J, Aliev F, Nurnberger J Jr, Kramer J, Kuperman S, Porjesz B, Tischfield J, Edenberg HJ, Foroud T, Schuckit M, Goate A, Hesselbrock V, Bierut L.

Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1179-88. doi: 10.1002/ajmg.b.31089.

PMID:: 20468071; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 1980774410.

Primary congenital glaucoma caused by the homozygous F261L CYP1B1 mutation and paternal isodisomy of chromosome 2.

López-Garrido MP, Campos-Mollo E, Harto MA, Escribano J.

Clin Genet. 2009 Dec;76(6):552-7. doi: 10.1111/j.1399-0004.2009.01242.x. Epub 2009 Oct 6.

PMID:: 19807744; [PubMed - indexed for MEDLINE]

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Select item 1980513211.

Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados.

Jiao X, Yang Z, Yang X, Chen Y, Tong Z, Zhao C, Zeng J, Chen H, Gibbs D, Sun X, Li B, Wakins WS, Meyer C, Wang X, Kasuga D, Bedell M, Pearson E, Weinreb RN, Leske MC, Hennis A, DeWan A, Nemesure B, Jorde LB, Hoh J, Hejtmancik JF, Zhang K.

Proc Natl Acad Sci U S A. 2009 Oct 6;106(40):17105-10. doi: 10.1073/pnas.0907564106. Epub 2009 Sep 24.

PMID:: 19805132; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 1973764812.

Amplification of the ABCB1 region accompanied by a short sequence of 200bp from chromosome 2 in lung cancer cells.

Kitada K, Yamasaki T, Aikawa S.

Cancer Genet Cytogenet. 2009 Oct;194(1):4-11. doi: 10.1016/j.cancergencyto.2009.05.002.

PMID:: 19737648; [PubMed - indexed for MEDLINE]

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Select item 1966570413.

Is classic pericentric inversion of chromosome 2 inv(2)(p11q13) associated with an increased risk of unbalanced chromosomes?

Ferfouri F, Clement P, Gomes DM, Minz M, Amar E, Selva J, Vialard F.

Fertil Steril. 2009 Oct;92(4):1497.e1-4. doi: 10.1016/j.fertnstert.2009.06.047. Epub 2009 Aug 8.

PMID:: 19665704; [PubMed - indexed for MEDLINE]

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Select item 1961011714.

Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.

Keller MC, McRae AF, McGaughran JM, Visscher PM, Martin NG, Montgomery GW.

Am J Med Genet A. 2009 Aug;149A(8):1823-6. doi: 10.1002/ajmg.a.32973. No abstract available.

PMID:: 19610117; [PubMed - indexed for MEDLINE]

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Select item 1952134815.

Evidence for three novel QTLs for adiposity on chromosome 2 with epistatic interactions: the NHLBI Family Heart Study.

Feitosa MF, North KE, Myers RH, Pankow JS, Borecki IB.

Obesity (Silver Spring). 2009 Dec;17(12):2190-5. doi: 10.1038/oby.2009.181. Epub 2009 Jun 11.

PMID:: 19521348; [PubMed - indexed for MEDLINE]

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Select item 1940647316.

Gain of the short arm of chromosome 2 (2p) is a frequent recurring chromosome aberration in untreated chronic lymphocytic leukemia (CLL) at advanced stages.

Chapiro E, Leporrier N, Radford-Weiss I, Bastard C, Mossafa H, Leroux D, Tigaud I, De Braekeleer M, Terré C, Brizard F, Callet-Bauchu E, Struski S, Veronese L, Fert-Ferrer S, Taviaux S, Lesty C, Davi F, Merle-Béral H, Bernard OA, Sutton L, Raynaud SD, Nguyen-Khac F.

Leuk Res. 2010 Jan;34(1):63-8. doi: 10.1016/j.leukres.2009.03.042. Epub 2009 Apr 29.

PMID:: 19406473; [PubMed - indexed for MEDLINE]

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3 free full-text articles in PubMed Central

The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2. [Genome Res. 2012]
The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2.
Ventura M, Catacchio CR, Sajjadian S, Vives L, Sudmant PH, Marques-Bonet T, Graves TA, Wilson RK, Eichler EE. Genome Res. 2012 Jun; 22(6):1036-49. Epub 2012 Mar 14.
Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts. [Am J Med Genet B Neuropsychiat...]
Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts.
Dick DM, Meyers J, Aliev F, Nurnberger J Jr, Kramer J, Kuperman S, Porjesz B, Tischfield J, Edenberg HJ, Foroud T, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Sep; 153B(6):1179-88.
Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados. [Proc Natl Acad Sci U S A. 2009]
Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados.
Jiao X, Yang Z, Yang X, Chen Y, Tong Z, Zhao C, Zeng J, Chen H, Gibbs D, Sun X, et al. Proc Natl Acad Sci U S A. 2009 Oct 6; 106(40):17105-10. Epub 2009 Sep 24.

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