175 related articles for article (PubMed ID: 20101690)
1. Two siblings with alternate unbalanced recombinants derived from a large cryptic maternal pericentric inversion of chromosome 20.
Descipio C; Morrissette JD; Conlin LK; Clark D; Kaur M; Coplan J; Riethman H; Spinner NB; Krantz ID
Am J Med Genet A; 2010 Feb; 152A(2):373-82. PubMed ID: 20101690
[TBL] [Abstract][Full Text] [Related]
2. Identical cryptic partial monosomy 20pter and trisomy 20qter in three adult siblings due to a large maternal pericentric inversion: detection by MLPA and breakpoint mapping by SNP array analysis.
Stevens SJ; Smeets EE; Blom E; van Uum CM; Albrechts JC; Herbergs J; Janssen JW; Engelen JJ
Am J Med Genet A; 2009 Oct; 149A(10):2226-30. PubMed ID: 19725130
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 20684015
[TBL] [Abstract][Full Text] [Related]
4. Cytogenetic and molecular cytogenetic findings in 43 aneurysmal bone cysts: aberrations of 17p mapped to 17p13.2 by fluorescence in situ hybridization.
Althof PA; Ohmori K; Zhou M; Bailey JM; Bridge RS; Nelson M; Neff JR; Bridge JA
Mod Pathol; 2004 May; 17(5):518-25. PubMed ID: 15044915
[TBL] [Abstract][Full Text] [Related]
5. Intrachromosomal insertion mimicking a pericentric inversion: molecular cytogenetic characterization of a three break rearrangement of chromosome 20.
Ardalan A; Prieur M; Choiset A; Turleau C; Goutieres F; Girard-Orgeolet S
Am J Med Genet A; 2005 Oct; 138A(3):288-93. PubMed ID: 16158442
[TBL] [Abstract][Full Text] [Related]
6. Recombination aneusomy of subtelomeric regions of chromosome 5, resulting from a large familial pericentric inversion inv(5)(p15.33q35.3).
Bocian E; Suchenek K; Obersztyn E; Nowakowska B; Mazurczak T
J Appl Genet; 2005; 46(1):109-14. PubMed ID: 15741672
[TBL] [Abstract][Full Text] [Related]
7. Cryptic duplication of 12q24.33 --> qter in a child with Angelman syndrome-simultaneous occurrence of two unrelated cytogenetic events.
Sathanoori M; Hu J; Murthy V; Byrnes A; Vockley J; Safier R; Bedoyan J; Jalal SM; Huber H; Surti U
Am J Med Genet A; 2007 May; 143A(9):985-94. PubMed ID: 17394213
[TBL] [Abstract][Full Text] [Related]
8. Duplication of distal 20q: clinical, cytogenetic and array CGH. Characterization of a new case.
Iglesias A; Rauen KA; Albertson DG; Pinkel D; Cotter PD
Clin Dysmorphol; 2006 Jan; 15(1):19-23. PubMed ID: 16317302
[TBL] [Abstract][Full Text] [Related]
9. A father and son with mental retardation, a characteristic face, inv(12), and insertion trisomy 12p12.3-p11.2.
Liang D; Wu L; Pan Q; Harada N; Long Z; Xia K; Yoshiura K; Dai H; Niikawa N; Cai F; Xia J
Am J Med Genet A; 2006 Feb; 140(3):238-44. PubMed ID: 16411213
[TBL] [Abstract][Full Text] [Related]
10. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.
Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Lee MS; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420
[TBL] [Abstract][Full Text] [Related]
11. FISH studies identify the i(20q-) anomaly as a der(20)del(20)(q11q13)idic(20)(p11).
Li T; Xue Y; Wu Y; Pan J
Genes Chromosomes Cancer; 2006 Jun; 45(6):536-9. PubMed ID: 16506189
[TBL] [Abstract][Full Text] [Related]
12. Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion.
Zamani AG; Acar A; Durakbasi-Dursun G; Yildirim MS; Ceylaner S; Tuncez E
Am J Med Genet A; 2014 May; 164A(5):1239-44. PubMed ID: 24478222
[TBL] [Abstract][Full Text] [Related]
13. Chromosome arm 20q gains and other genomic alterations in colorectal cancer metastatic to liver, as analyzed by comparative genomic hybridization and fluorescence in situ hybridization.
Korn WM; Yasutake T; Kuo WL; Warren RS; Collins C; Tomita M; Gray J; Waldman FM
Genes Chromosomes Cancer; 1999 Jun; 25(2):82-90. PubMed ID: 10337990
[TBL] [Abstract][Full Text] [Related]
14. Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: clinical data and molecular characterization.
Schluth-Bolard C; Till M; Rafat A; Labalme A; Le Lorc'h M; Banquart E; Angei C; Cordier MP; Romana SP; Edery P; Sanlaville D
Eur J Med Genet; 2008; 51(6):622-30. PubMed ID: 18674648
[TBL] [Abstract][Full Text] [Related]
15. Molecular characterization of a novel, de novo, cryptic interstitial deletion on 19p13.3 in a child with a cutis aplasia and multiple congenital anomalies.
Al-Kateb H; Hahn A; Gastier-Foster JM; Jeng L; McCandless SE; Curtis CA
Am J Med Genet A; 2010 Dec; 152A(12):3148-53. PubMed ID: 21108400
[TBL] [Abstract][Full Text] [Related]
16. Update on "two siblings with alternate unbalanced recombinants derived from a large cryptic maternal pericentric inversion of chromosome 20".
Descipio C; Morrissette JD; Conlin LK; Clark D; Kaur M; Coplan J; Riethman H; Spinner NB; Krantz ID
Am J Med Genet A; 2010 Jun; 152A(6):1599. PubMed ID: 20503345
[No Abstract] [Full Text] [Related]
17. Duplication of 20qter and deletion of 20pter due to paternal pericentric inversion: patient report and review of 20qter duplications.
Starr LJ; Truemper EJ; Pickering DL; Sanger WG; Olney AH
Am J Med Genet A; 2014 Aug; 164A(8):2020-4. PubMed ID: 24954807
[TBL] [Abstract][Full Text] [Related]
18. Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4.
Cotter PD; Kaffe S; Li L; Gershin IF; Hirschhorn K
Am J Med Genet; 2001 Jul; 102(1):76-80. PubMed ID: 11471177
[TBL] [Abstract][Full Text] [Related]
19. Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.
Ravnan JB; Tepperberg JH; Papenhausen P; Lamb AN; Hedrick J; Eash D; Ledbetter DH; Martin CL
J Med Genet; 2006 Jun; 43(6):478-89. PubMed ID: 16199540
[TBL] [Abstract][Full Text] [Related]
20. Case of partial duplication 2q3 with characteristic phenotype: rare occurrence of an unbalanced offspring resulting from a parental pericentric inversion.
Angle B; Hersh JH; Yen F; Christensen KM
Am J Med Genet; 2000 Mar; 91(2):126-30. PubMed ID: 10748411
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
