These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

81 related articles for article (PubMed ID: 26884608)

  • 1. Unraveling De Novo Copy Number Variants in Congenital Heart Defects: The Bottom of the Iceberg Is Under Attack.
    Bouvagnet P
    Circ Cardiovasc Genet; 2016 Feb; 9(1):4-5. PubMed ID: 26884608
    [No Abstract]   [Full Text] [Related]  

  • 2. Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the Aorta.
    Sanchez-Castro M; Eldjouzi H; Charpentier E; Busson PF; Hauet Q; Lindenbaum P; Delasalle-Guyomarch B; Baudry A; Pichon O; Pascal C; Lefort B; Bajolle F; Pezard P; Schott JJ; Dina C; Redon R; Gournay V; Bonnet D; Le Caignec C
    Circ Cardiovasc Genet; 2016 Feb; 9(1):86-94. PubMed ID: 26643481
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [Analysis of genomic copy number variations in two unrelated neonates with 8p deletion and duplication associated with congenital heart disease].
    Mei M; Yang L; Zhan G; Wang H; Ma D; Zhou W; Huang G
    Zhonghua Er Ke Za Zhi; 2014 Jun; 52(6):460-3. PubMed ID: 25190168
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication.
    Pires R; Pires LM; Vaz SO; Maciel P; Anjos R; Moniz R; Branco CC; Cabral R; Carreira IM; Mota-Vieira L
    BMC Genet; 2014 Nov; 15():115. PubMed ID: 25376777
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Assessment of the role of copy-number variants in 150 patients with congenital heart defects.
    Derwińska K; Bartnik M; Wiśniowiecka-Kowalnik B; Jagła M; Rudziński A; Pietrzyk JJ; Kawalec W; Ziółkowska L; Kutkowska-Kaźmierczak A; Gambin T; Sykulski M; Shaw CA; Gambin A; Mazurczak T; Obersztyn E; Bocian E; Stankiewicz P
    Med Wieku Rozwoj; 2012; 16(3):175-82. PubMed ID: 23378395
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Copy number variants and the genetic enigma of congenital heart disease.
    Marian AJ
    Circ Res; 2014 Oct; 115(10):821-3. PubMed ID: 25342769
    [No Abstract]   [Full Text] [Related]  

  • 9. [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]  

  • 10. DNA copy number variations in patients with 46,XY disorders of sex development.
    Harrison SM; Granberg CF; Keays M; Hill M; Grimsby GM; Baker LA
    J Urol; 2014 Dec; 192(6):1801-6. PubMed ID: 24946221
    [TBL] [Abstract][Full Text] [Related]  

  • 11. No evidence for mosaic pathogenic copy number variations in cardiac tissue from patients with congenital heart malformations.
    Winberg J; Berggren H; Malm T; Johansson S; Johansson Ramgren J; Nilsson B; Liedén A; Nordenskjöld A; Gustavsson P; Nordgren A
    Eur J Med Genet; 2015 Mar; 58(3):129-33. PubMed ID: 25652018
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region.
    Yang YF; Ai Q; Huang C; Chen JL; Wang J; Xie L; Zhang WZ; Yang JF; Tan ZP
    Gene; 2013 Oct; 528(1):51-4. PubMed ID: 23639964
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Copy number variants in congenital heart disease: A new risk factor impacting outcomes?
    Lee TM; Bacha EA
    J Thorac Cardiovasc Surg; 2016 Apr; 151(4):1152-3. PubMed ID: 26515872
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Application of Array Comparative Genomic Hybridization in Newborns with Multiple Congenital Anomalies.
    Szczałuba K; Nowakowska B; Sobecka K; Smyk M; Castaneda J; Klapecki J; Kutkowska-Kaźmierczak A; Śmigiel R; Bocian E; Radkowski M; Demkow U
    Adv Exp Med Biol; 2016; 912():1-9. PubMed ID: 26987320
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromosomal abnormalities and copy number variations in fetal left-sided congenital heart defects.
    Jansen FA; Hoffer MJ; van Velzen CL; Plati SK; Rijlaarsdam ME; Clur SA; Blom NA; Pajkrt E; Bhola SL; Knegt AC; de Boer MA; Haak MC
    Prenat Diagn; 2016 Feb; 36(2):177-85. PubMed ID: 26716421
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Analysis of de novo copy number variations in a family affected with autism spectrum disorders using high-resolution array-based comparative genomic hybridization].
    He WZ; Liu WQ; Zhong XQ; Chen XL; Li SY; Zhang HM; Li Q; Cui QL; Sun XF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Jun; 29(3):266-9. PubMed ID: 22678785
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Rare Novel Copy Number Variation of Xp22.33-p11.22 Duplication is Associated with Congenital Heart Defects.
    Zhang J; Wu QQ; Wang L; Sun LJ
    Chin Med J (Engl); 2015 Oct; 128(20):2829-30. PubMed ID: 26481757
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.