62 related articles for article (PubMed ID: 11511922)
1. The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers.
Tapia-Páez I; Kost-Alimova M; Hu P; Roe BA; Blennow E; Fedorova L; Imreh S; Dumanski JP
Hum Genet; 2001 Aug; 109(2):167-77. PubMed ID: 11511922
[TBL] [Abstract][Full Text] [Related]
2. Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.
Ou Z; Stankiewicz P; Xia Z; Breman AM; Dawson B; Wiszniewska J; Szafranski P; Cooper ML; Rao M; Shao L; South ST; Coleman K; Fernhoff PM; Deray MJ; Rosengren S; Roeder ER; Enciso VB; Chinault AC; Patel A; Kang SH; Shaw CA; Lupski JR; Cheung SW
Genome Res; 2011 Jan; 21(1):33-46. PubMed ID: 21205869
[TBL] [Abstract][Full Text] [Related]
3. Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia.
Velagaleti GV; Bien-Willner GA; Northup JK; Lockhart LH; Hawkins JC; Jalal SM; Withers M; Lupski JR; Stankiewicz P
Am J Hum Genet; 2005 Apr; 76(4):652-62. PubMed ID: 15726498
[TBL] [Abstract][Full Text] [Related]
4. The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats.
Kurahashi H; Shaikh T; Takata M; Toda T; Emanuel BS
Am J Hum Genet; 2003 Mar; 72(3):733-8. PubMed ID: 12557125
[TBL] [Abstract][Full Text] [Related]
5. Rapid mapping of chromosomal breakpoints: from blood to BAC in 20 days.
Lu CM; Kwan J; Weier JF; Baumgartner A; Wang M; Escudero T; Munné S; Weier HU
Folia Histochem Cytobiol; 2009 Jan; 47(3):367-75. PubMed ID: 20164020
[TBL] [Abstract][Full Text] [Related]
6. Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis.
Weckselblatt B; Hermetz KE; Rudd MK
Genome Res; 2015 Jul; 25(7):937-47. PubMed ID: 26070663
[TBL] [Abstract][Full Text] [Related]
7. Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition.
Varley H; Di S; Scherer SW; Royle NJ
Am J Hum Genet; 2000 Sep; 67(3):610-22. PubMed ID: 10924407
[TBL] [Abstract][Full Text] [Related]
8. Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation.
Nilsson D; Pettersson M; Gustavsson P; Förster A; Hofmeister W; Wincent J; Zachariadis V; Anderlid BM; Nordgren A; Mäkitie O; Wirta V; Käller M; Vezzi F; Lupski JR; Nordenskjöld M; Lundberg ES; Carvalho CMB; Lindstrand A
Hum Mutat; 2017 Feb; 38(2):180-192. PubMed ID: 27862604
[TBL] [Abstract][Full Text] [Related]
9. Genome architecture catalyzes nonrecurrent chromosomal rearrangements.
Stankiewicz P; Shaw CJ; Dapper JD; Wakui K; Shaffer LG; Withers M; Elizondo L; Park SS; Lupski JR
Am J Hum Genet; 2003 May; 72(5):1101-16. PubMed ID: 12649807
[TBL] [Abstract][Full Text] [Related]
10. A constitutional translocation t(1;17)(p36.2;q11.2) in a neuroblastoma patient disrupts the human NBPF1 and ACCN1 genes.
Vandepoele K; Andries V; Van Roy N; Staes K; Vandesompele J; Laureys G; De Smet E; Berx G; Speleman F; van Roy F
PLoS One; 2008 May; 3(5):e2207. PubMed ID: 18493581
[TBL] [Abstract][Full Text] [Related]
11. Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins.
Johnson D; Morrison N; Grant L; Turner T; Fantes J; Connor JM; Murday V
J Med Genet; 2006 Mar; 43(3):280-4. PubMed ID: 16118347
[TBL] [Abstract][Full Text] [Related]
12. DNA probe pooling for rapid delineation of chromosomal breakpoints.
Lu CM; Kwan J; Baumgartner A; Weier JF; Wang M; Escudero T; Munné S; Zitzelsberger HF; Weier HU
J Histochem Cytochem; 2009 Jun; 57(6):587-97. PubMed ID: 19223294
[TBL] [Abstract][Full Text] [Related]
13. Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome.
Shi W; Massaia A; Louzada S; Handsaker J; Chow W; McCarthy S; Collins J; Hallast P; Howe K; Church DM; Yang F; Xue Y; Tyler-Smith C
Genome Biol; 2019 Oct; 20(1):207. PubMed ID: 31610793
[TBL] [Abstract][Full Text] [Related]
14. Haploinsufficiency of ARHGAP42 is associated with hypertension.
Fjorder AS; Rasmussen MB; Mehrjouy MM; Nazaryan-Petersen L; Hansen C; Bak M; Grarup N; Nørremølle A; Larsen LA; Vestergaard H; Hansen T; Tommerup N; Bache I
Eur J Hum Genet; 2019 Aug; 27(8):1296-1303. PubMed ID: 30903111
[TBL] [Abstract][Full Text] [Related]
15. Genetic variation affects de novo translocation frequency.
Kato T; Inagaki H; Yamada K; Kogo H; Ohye T; Kowa H; Nagaoka K; Taniguchi M; Emanuel BS; Kurahashi H
Science; 2006 Feb; 311(5763):971. PubMed ID: 16484486
[TBL] [Abstract][Full Text] [Related]
16. The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.
Kurahashi H; Inagaki H; Ohye T; Kogo H; Tsutsumi M; Kato T; Tong M; Emanuel BS
Clin Genet; 2010 Oct; 78(4):299-309. PubMed ID: 20507342
[TBL] [Abstract][Full Text] [Related]
17. Characterization of chromosome 11 breakpoints and the areas of deletion and amplification in patients with newly diagnosed acute myeloid leukemia.
Sarova I; Brezinova J; Zemanova Z; Bystricka D; Krejcik Z; Soukup P; Vydra J; Cermak J; Jonasova A; Michalova K
Genes Chromosomes Cancer; 2013 Jul; 52(7):619-35. PubMed ID: 23580398
[TBL] [Abstract][Full Text] [Related]
18. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation.
Hou JW
Chang Gung Med J; 2003 Jan; 26(1):48-52. PubMed ID: 12656309
[TBL] [Abstract][Full Text] [Related]
19. Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements.
Inagaki H; Kato T; Tsutsumi M; Ouchi Y; Ohye T; Kurahashi H
Front Genet; 2016; 7():125. PubMed ID: 27462347
[TBL] [Abstract][Full Text] [Related]
20. Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation.
Mishra D; Kato T; Inagaki H; Kosho T; Wakui K; Kido Y; Sakazume S; Taniguchi-Ikeda M; Morisada N; Iijima K; Fukushima Y; Emanuel BS; Kurahashi H
Mol Cytogenet; 2014; 7():55. PubMed ID: 25478009
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
