158 related articles for article (PubMed ID: 35328767)
1. Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region.
Redaelli S; Conconi D; Sala E; Villa N; Crosti F; Roversi G; Catusi I; Valtorta C; Recalcati MP; Dalprà L; Lavitrano M; Bentivegna A
Int J Mol Sci; 2022 Mar; 23(6):. PubMed ID: 35328767
[TBL] [Abstract][Full Text] [Related]
2. Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2.
Giorda R; Ciccone R; Gimelli G; Pramparo T; Beri S; Bonaglia MC; Giglio S; Genuardi M; Argente J; Rocchi M; Zuffardi O
Hum Mutat; 2007 May; 28(5):459-68. PubMed ID: 17262805
[TBL] [Abstract][Full Text] [Related]
3. Comparative genomic hybridization, allelic imbalance, and fluorescence in situ hybridization on chromosome 8 in prostate cancer.
Cher ML; MacGrogan D; Bookstein R; Brown JA; Jenkins RB; Jensen RH
Genes Chromosomes Cancer; 1994 Nov; 11(3):153-62. PubMed ID: 7530484
[TBL] [Abstract][Full Text] [Related]
4. High-resolution array CGH clarifies events occurring on 8p in carcinogenesis.
Cooke SL; Pole JC; Chin SF; Ellis IO; Caldas C; Edwards PA
BMC Cancer; 2008 Oct; 8():288. PubMed ID: 18840272
[TBL] [Abstract][Full Text] [Related]
5. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH
Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814
[TBL] [Abstract][Full Text] [Related]
6. Cytogenetic and fluorescence in situ hybridization characterization of chromosome 8 rearrangements in head and neck squamous cell carcinomas.
Jin Y; Jin C; Wennerberg J; Höglund M; Mertens F
Cancer Genet Cytogenet; 2001 Oct; 130(2):111-7. PubMed ID: 11675131
[TBL] [Abstract][Full Text] [Related]
7. Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement.
Cooke SL; Northup JK; Champaige NL; Zinser W; Edwards PA; Lockhart LH; Velagaleti GV
Am J Med Genet A; 2008 May; 146A(9):1166-72. PubMed ID: 18302246
[TBL] [Abstract][Full Text] [Related]
8. Unusual 8p inverted duplication deletion with telomere capture from 8q.
Buysse K; Antonacci F; Callewaert B; Loeys B; Fränkel U; Siu V; Mortier G; Speleman F; Menten B
Eur J Med Genet; 2009; 52(1):31-6. PubMed ID: 19041960
[TBL] [Abstract][Full Text] [Related]
9. Characterization of a complex rearrangement of a chromosome 20 by FISH and array CGH.
Bertini V; Valetto A; Baroncelli GI; Simi P
Eur J Med Genet; 2011; 54(4):e419-24. PubMed ID: 21440097
[TBL] [Abstract][Full Text] [Related]
10. Characterization of genetic rearrangements in esophageal squamous carcinoma cell lines by a combination of M-FISH and array-CGH: further confirmation of some split genomic regions in primary tumors.
Hao JJ; Shi ZZ; Zhao ZX; Zhang Y; Gong T; Li CX; Zhan T; Cai Y; Dong JT; Fu SB; Zhan QM; Wang MR
BMC Cancer; 2012 Aug; 12():367. PubMed ID: 22920630
[TBL] [Abstract][Full Text] [Related]
11. Complex CGH alterations on chromosome arm 8p at candidate tumor suppressor gene loci in breast cancer cell lines.
Venter DJ; Ramus SJ; Hammet FM; de Silva M; Hutchins AM; Petrovic V; Price G; Armes JE
Cancer Genet Cytogenet; 2005 Jul; 160(2):134-40. PubMed ID: 15993269
[TBL] [Abstract][Full Text] [Related]
12. A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones.
Popp S; Jauch A; Schindler D; Speicher MR; Lengauer C; Donis-Keller H; Riethman HC; Cremer T
Hum Genet; 1993 Dec; 92(6):527-32. PubMed ID: 8262510
[TBL] [Abstract][Full Text] [Related]
13. U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangements.
Rowe LR; Lee JY; Rector L; Kaminsky EB; Brothman AR; Martin CL; South ST
J Med Genet; 2009 Oct; 46(10):694-702. PubMed ID: 19293169
[TBL] [Abstract][Full Text] [Related]
14. Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators?
Redaelli S; Grati FR; Tritto V; Giannuzzi G; Recalcati MP; Sala E; Villa N; Crosti F; Roversi G; Malvestiti F; Zanatta V; Repetti E; Rodeschini O; Valtorta C; Catusi I; Romitti L; Martinoli E; Conconi D; Dalprà L; Lavitrano M; Riva P; Bentivegna A
HGG Adv; 2024 Apr; 5(2):100261. PubMed ID: 38160254
[TBL] [Abstract][Full Text] [Related]
15. Clinical array-based karyotyping of breast cancer with equivocal HER2 status resolves gene copy number and reveals chromosome 17 complexity.
Gunn S; Yeh IT; Lytvak I; Tirtorahardjo B; Dzidic N; Zadeh S; Kim J; McCaskill C; Lim L; Gorre M; Mohammed M
BMC Cancer; 2010 Jul; 10():396. PubMed ID: 20667129
[TBL] [Abstract][Full Text] [Related]
16. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
[TBL] [Abstract][Full Text] [Related]
17. Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?
Bejjani BA; Saleki R; Ballif BC; Rorem EA; Sundin K; Theisen A; Kashork CD; Shaffer LG
Am J Med Genet A; 2005 Apr; 134(3):259-67. PubMed ID: 15723295
[TBL] [Abstract][Full Text] [Related]
18. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
Schluth-Bolard C; Delobel B; Sanlaville D; Boute O; Cuisset JM; Sukno S; Labalme A; Duban-Bedu B; Plessis G; Jaillard S; Dubourg C; Henry C; Lucas J; Odent S; Pasquier L; Copin H; Latour P; Cordier MP; Nadeau G; Till M; Edery P; Andrieux J
Eur J Med Genet; 2009; 52(5):291-6. PubMed ID: 19505601
[TBL] [Abstract][Full Text] [Related]
19. Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.
Sireteanu A; Braha E; Popescu R; Gramescu M; Gorduza EV; Rusu C
Rev Med Chir Soc Med Nat Iasi; 2013; 117(3):731-4. PubMed ID: 24502041
[TBL] [Abstract][Full Text] [Related]
20. [Balanced chromosomal rearrangements resulting in intellectual disability. An analysis of 22 cases with application of CGH and FISH methods].
Borg K; Bocian E; Bernaciak J; Nowakowska B; Derwińska K; Obersztyn E; Szczałuba K; Smigiel R; Kostyk E; Mazurczak T
Med Wieku Rozwoj; 2009; 13(2):81-93. PubMed ID: 19837989
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
