124 related articles for article (PubMed ID: 20138633)
1. Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects.
Breckpot J; Thienpont B; Peeters H; de Ravel T; Singer A; Rayyan M; Allegaert K; Vanhole C; Eyskens B; Vermeesch JR; Gewillig M; Devriendt K
J Pediatr; 2010 May; 156(5):810-7, 817.e1-817.e4. PubMed ID: 20138633
[TBL] [Abstract][Full Text] [Related]
2. Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defects.
Breckpot J; Thienpont B; Arens Y; Tranchevent LC; Vermeesch JR; Moreau Y; Gewillig M; Devriendt K
Cytogenet Genome Res; 2011; 135(3-4):251-9. PubMed ID: 21921585
[TBL] [Abstract][Full Text] [Related]
3. Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients.
Thienpont B; Mertens L; de Ravel T; Eyskens B; Boshoff D; Maas N; Fryns JP; Gewillig M; Vermeesch JR; Devriendt K
Eur Heart J; 2007 Nov; 28(22):2778-84. PubMed ID: 17384091
[TBL] [Abstract][Full Text] [Related]
4. Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis.
Jansen FA; Blumenfeld YJ; Fisher A; Cobben JM; Odibo AO; Borrell A; Haak MC
Ultrasound Obstet Gynecol; 2015 Jan; 45(1):27-35. PubMed ID: 25319878
[TBL] [Abstract][Full Text] [Related]
5. Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis.
Yu S; Bittel DC; Kibiryeva N; Zwick DL; Cooley LD
Am J Clin Pathol; 2009 Sep; 132(3):349-60. PubMed ID: 19687311
[TBL] [Abstract][Full Text] [Related]
6. High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.
Erdogan F; Larsen LA; Zhang L; Tümer Z; Tommerup N; Chen W; Jacobsen JR; Schubert M; Jurkatis J; Tzschach A; Ropers HH; Ullmann R
J Med Genet; 2008 Nov; 45(11):704-9. PubMed ID: 18713793
[TBL] [Abstract][Full Text] [Related]
7. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
Yan Y; Wu Q; Zhang L; Wang X; Dan S; Deng D; Sun L; Yao L; Ma Y; Wang L
Ultrasound Obstet Gynecol; 2014 Apr; 43(4):404-12. PubMed ID: 24323407
[TBL] [Abstract][Full Text] [Related]
8. Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization.
Fan YS; Jayakar P; Zhu H; Barbouth D; Sacharow S; Morales A; Carver V; Benke P; Mundy P; Elsas LJ
Hum Mutat; 2007 Nov; 28(11):1124-32. PubMed ID: 17621639
[TBL] [Abstract][Full Text] [Related]
9. Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease.
Syrmou A; Tzetis M; Fryssira H; Kosma K; Oikonomakis V; Giannikou K; Makrythanasis P; Kitsiou-Tzeli S; Kanavakis E
Pediatr Res; 2013 Jun; 73(6):772-6. PubMed ID: 23481551
[TBL] [Abstract][Full Text] [Related]
10. Array comparative genomic hybridisation testing in CHD.
Hightower HB; Robin NH; Mikhail FM; Ambalavanan N
Cardiol Young; 2015 Aug; 25(6):1155-72. PubMed ID: 25296170
[TBL] [Abstract][Full Text] [Related]
11. Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies.
Hayashi S; Imoto I; Aizu Y; Okamoto N; Mizuno S; Kurosawa K; Okamoto N; Honda S; Araki S; Mizutani S; Numabe H; Saitoh S; Kosho T; Fukushima Y; Mitsubuchi H; Endo F; Chinen Y; Kosaki R; Okuyama T; Ohki H; Yoshihashi H; Ono M; Takada F; Ono H; Yagi M; Matsumoto H; Makita Y; Hata A; Inazawa J
J Hum Genet; 2011 Feb; 56(2):110-24. PubMed ID: 20981036
[TBL] [Abstract][Full Text] [Related]
12. High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical setting.
Wincent J; Anderlid BM; Lagerberg M; Nordenskjöld M; Schoumans J
Clin Genet; 2011 Feb; 79(2):147-57. PubMed ID: 20486943
[TBL] [Abstract][Full Text] [Related]
13. The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization.
Tzetis M; Kitsiou-Tzeli S; Frysira H; Xaidara A; Kanavakis E
Expert Rev Mol Diagn; 2012 Jun; 12(5):449-57. PubMed ID: 22702362
[TBL] [Abstract][Full Text] [Related]
14. Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation.
Gekas J; Vallée M; Castonguay L; Laframboise R; Maranda B; Piedboeuf B; Rousseau F
J Med Genet; 2011 Dec; 48(12):851-5. PubMed ID: 21965346
[TBL] [Abstract][Full Text] [Related]
15. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.
Law LW; Lau TK; Fung TY; Leung TY; Wang CC; Choy KW
BJOG; 2009 Jan; 116(2):339-43. PubMed ID: 19018765
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. [Detection of cryptic copy number variations in a fetus with congenital heart disease by array-based comparative genomic hybridization].
HU P; WANG Y; JI XQ; LIN Y; Li L; ZHOU XY; CHEN J; MA DY; CAO L; Xu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):133-6. PubMed ID: 21462121
[TBL] [Abstract][Full Text] [Related]
19. [Fetal chromosome technique by microarray-based comparative genomic hybridization].
Jonveaux P
Arch Pediatr; 2010 Jul; 17(7):1119-23. PubMed ID: 20347579
[TBL] [Abstract][Full Text] [Related]
20. Genomic alterations of chromosome region 11p as predictive marker by array comparative genomic hybridization in lung adenocarcinoma patients.
Sung JS; Park KH; Kim YH
Cancer Genet Cytogenet; 2010 Apr; 198(1):27-34. PubMed ID: 20303011
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]