254 related articles for article (PubMed ID: 21921585)
1. 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]
2. 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]
3. 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]
4. 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]
5. [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]
6. High resolution array in the clinical approach to chromosomal phenotypes.
Filges I; Suda L; Weber P; Datta AN; Fischer D; Dill P; Glanzmann R; Benzing J; Hegi L; Wenzel F; Huber AR; Mori AC; Miny P; Röthlisberger B
Gene; 2012 Mar; 495(2):163-9. PubMed ID: 22240311
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Cytogenomic Evaluation of Subjects with Syndromic and Nonsyndromic Conotruncal Heart Defects.
de Souza KR; Mergener R; Huber J; Campos Pellanda L; Riegel M
Biomed Res Int; 2015; 2015():401941. PubMed ID: 26137477
[TBL] [Abstract][Full Text] [Related]
9. Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
Geng J; Picker J; Zheng Z; Zhang X; Wang J; Hisama F; Brown DW; Mullen MP; Harris D; Stoler J; Seman A; Miller DT; Fu Q; Roberts AE; Shen Y
BMC Genomics; 2014 Dec; 15(1):1127. PubMed ID: 25516202
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. [Chromosomal changes in congenital heart disease].
Larsen LA
Ugeskr Laeger; 2011 Jan; 173(3):194-6. PubMed ID: 21241627
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
Cappuccio G; Vitiello F; Casertano A; Fontana P; Genesio R; Bruzzese D; Ginocchio VM; Mormile A; Nitsch L; Andria G; Melis D
Ital J Pediatr; 2016 Apr; 42():39. PubMed ID: 27072107
[TBL] [Abstract][Full Text] [Related]
15. Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience.
Buysse K; Delle Chiaie B; Van Coster R; Loeys B; De Paepe A; Mortier G; Speleman F; Menten B
Eur J Med Genet; 2009; 52(6):398-403. PubMed ID: 19765681
[TBL] [Abstract][Full Text] [Related]
16. Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases.
Nagy O; Szakszon K; Biró BO; Mogyorósy G; Nagy D; Nagy B; Balogh I; Ujfalusi A
J Biotechnol; 2019 Jun; 299():86-95. PubMed ID: 31054299
[TBL] [Abstract][Full Text] [Related]
17. A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
Zhang X; Xu Y; Liu D; Geng J; Chen S; Jiang Z; Fu Q; Sun K
BMC Genomics; 2015 May; 16(1):364. PubMed ID: 25952753
[TBL] [Abstract][Full Text] [Related]
18. Interpretation of array comparative genome hybridization data: a major challenge.
Gijsbers AC; Schoumans J; Ruivenkamp CA
Cytogenet Genome Res; 2011; 135(3-4):222-7. PubMed ID: 22086107
[TBL] [Abstract][Full Text] [Related]
19. High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease.
Zhao W; Niu G; Shen B; Zheng Y; Gong F; Wang X; Lee J; Mulvihill JJ; Chen X; Li S
Am J Med Genet A; 2013 Dec; 161A(12):3087-94. PubMed ID: 24115576
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
