197 related articles for article (PubMed ID: 20236111)
1. Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH.
Lindstrand A; Schoumans J; Gustavsson P; Hanemaaijer N; Malmgren H; Blennow E
Clin Genet; 2010 Jun; 77(6):552-62. PubMed ID: 20236111
[TBL] [Abstract][Full Text] [Related]
2. Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.
Selzer RR; Richmond TA; Pofahl NJ; Green RD; Eis PS; Nair P; Brothman AR; Stallings RL
Genes Chromosomes Cancer; 2005 Nov; 44(3):305-19. PubMed ID: 16075461
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
Simovich MJ; Yatsenko SA; Kang SH; Cheung SW; Dudek ME; Pursley A; Ward PA; Patel A; Lupski JR
Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
[TBL] [Abstract][Full Text] [Related]
4. Fine-tiling array CGH to improve diagnostics for α- and β-thalassemia rearrangements.
Phylipsen M; Chaibunruang A; Vogelaar IP; Balak JR; Schaap RA; Ariyurek Y; Fucharoen S; den Dunnen JT; Giordano PC; Bakker E; Harteveld CL
Hum Mutat; 2012 Jan; 33(1):272-80. PubMed ID: 21922597
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
[TBL] [Abstract][Full Text] [Related]
7. Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individuals.
Baptista J; Prigmore E; Gribble SM; Jacobs PA; Carter NP; Crolla JA
Eur J Hum Genet; 2005 Nov; 13(11):1205-12. PubMed ID: 16118644
[TBL] [Abstract][Full Text] [Related]
8. The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.
Gribble SM; Prigmore E; Burford DC; Porter KM; Ng BL; Douglas EJ; Fiegler H; Carr P; Kalaitzopoulos D; Clegg S; Sandstrom R; Temple IK; Youings SA; Thomas NS; Dennis NR; Jacobs PA; Crolla JA; Carter NP
J Med Genet; 2005 Jan; 42(1):8-16. PubMed ID: 15635069
[TBL] [Abstract][Full Text] [Related]
9. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
del Gaudio D; Yang Y; Boggs BA; Schmitt ES; Lee JA; Sahoo T; Pham HT; Wiszniewska J; Chinault AC; Beaudet AL; Eng CM
Hum Mutat; 2008 Sep; 29(9):1100-7. PubMed ID: 18752307
[TBL] [Abstract][Full Text] [Related]
10. Genomic alterations in myeloid neoplasms with novel, apparently balanced translocations.
Poitras JL; Costa D; Kluk MJ; Amrein PC; Stone RM; Lee C; Dal Cin P; Morton CC
Cancer Genet; 2011 Feb; 204(2):68-76. PubMed ID: 21504705
[TBL] [Abstract][Full Text] [Related]
11. 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation.
Malan V; Raoul O; Firth HV; Royer G; Turleau C; Bernheim A; Willatt L; Munnich A; Vekemans M; Lyonnet S; Cormier-Daire V; Colleaux L
J Med Genet; 2009 Sep; 46(9):635-40. PubMed ID: 19126570
[TBL] [Abstract][Full Text] [Related]
12. Rapid high-resolution mapping of balanced chromosomal rearrangements on tiling CGH arrays.
Greisman HA; Hoffman NG; Yi HS
J Mol Diagn; 2011 Nov; 13(6):621-33. PubMed ID: 21907824
[TBL] [Abstract][Full Text] [Related]
13. Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
Schoumans J; Ruivenkamp C; Holmberg E; Kyllerman M; Anderlid BM; Nordenskjöld M
J Med Genet; 2005 Sep; 42(9):699-705. PubMed ID: 16141005
[TBL] [Abstract][Full Text] [Related]
14. Characterisation of hairy cell leukaemia by tiling resolution array-based comparative genome hybridisation: a series of 13 cases and review of the literature.
Nordgren A; Corcoran M; Sääf A; Bremer A; Kluin-Nelemans HC; Schoumans J; Grandér D
Eur J Haematol; 2010 Jan; 84(1):17-25. PubMed ID: 19682064
[TBL] [Abstract][Full Text] [Related]
15. Breakpoint mapping by next generation sequencing reveals causative gene disruption in patients carrying apparently balanced chromosome rearrangements with intellectual deficiency and/or congenital malformations.
Schluth-Bolard C; Labalme A; Cordier MP; Till M; Nadeau G; Tevissen H; Lesca G; Boutry-Kryza N; Rossignol S; Rocas D; Dubruc E; Edery P; Sanlaville D
J Med Genet; 2013 Mar; 50(3):144-50. PubMed ID: 23315544
[TBL] [Abstract][Full Text] [Related]
16. Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromes.
Johnston JJ; Walker RL; Davis S; Facio F; Turner JT; Bick DP; Daentl DL; Ellison JW; Meltzer PS; Biesecker LG
J Med Genet; 2007 Jan; 44(1):e59. PubMed ID: 17098889
[TBL] [Abstract][Full Text] [Related]
17. Array painting using microdissected chromosomes to map chromosomal breakpoints.
Backx L; Van Esch H; Melotte C; Kosyakova N; Starke H; Frijns JP; Liehr T; Vermeesch JR
Cytogenet Genome Res; 2007; 116(3):158-66. PubMed ID: 17317954
[TBL] [Abstract][Full Text] [Related]
18. Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.
Yu W; Ballif BC; Kashork CD; Heilstedt HA; Howard LA; Cai WW; White LD; Liu W; Beaudet AL; Bejjani BA; Shaw CA; Shaffer LG
Hum Mol Genet; 2003 Sep; 12(17):2145-52. PubMed ID: 12915473
[TBL] [Abstract][Full Text] [Related]
19. Utility of array comparative genomic hybridization in cytogenetic analysis.
Singh RR; Cheung KJ; Horsman DE
Methods Mol Biol; 2011; 730():219-34. PubMed ID: 21431645
[TBL] [Abstract][Full Text] [Related]
20. Novel mechanisms of gene disruption at the medulloblastoma isodicentric 17p11 breakpoint.
McCabe MG; Ichimura K; Pearson DM; Liu L; Clifford SC; Ellison DW; Collins VP
Genes Chromosomes Cancer; 2009 Feb; 48(2):121-31. PubMed ID: 18973140
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
