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 *

144 related articles for article (PubMed ID: 28924535)

  • 1. Benign, Pathogenic and Copy Number Variations of Unknown Clinical Significance in Patients with Congenital Malformations and Developmental Delay.
    Mihaylova M; Staneva R; Toncheva D; Pancheva M; Hadjidekova S
    Balkan J Med Genet; 2017 Jun; 20(1):5-12. PubMed ID: 28924535
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability.
    Peycheva V; Kamenarova K; Ivanova N; Stamatov D; Avdjieva-Tzavella D; Alexandrova I; Zhelyazkova S; Pacheva I; Dimova P; Ivanov I; Litvinenko I; Bozhinova V; Tournev I; Simeonov E; Mitev V; Jordanova A; Kaneva R
    Gene; 2018 Aug; 667():45-55. PubMed ID: 29753047
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.
    Wayhelova M; Smetana J; Vallova V; Hladilkova E; Filkova H; Hanakova M; Vilemova M; Nikolova P; Gromesova B; Gaillyova R; Kuglik P
    BMC Med Genomics; 2019 Jul; 12(1):111. PubMed ID: 31337399
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Chromosomal microarray in clinical diagnosis: a study of 337 patients with congenital anomalies and developmental delays or intellectual disability.
    Sansović I; Ivankov AM; Bobinec A; Kero M; Barišić I
    Croat Med J; 2017 Jun; 58(3):231-238. PubMed ID: 28613040
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients.
    Perovic D; Damnjanovic T; Jekic B; Dusanovic-Pjevic M; Grk M; Djuranovic A; Rasic M; Novakovic I; Maksimovic N
    J Clin Lab Anal; 2022 Jun; 36(6):e24441. PubMed ID: 35441737
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan.
    Lee CL; Lee CH; Chuang CK; Chiu HC; Chen YJ; Chou CL; Wu PS; Chen CP; Lin HY; Lin SP
    Pediatr Neonatol; 2019 Aug; 60(4):453-460. PubMed ID: 30581099
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies.
    Maini I; Ivanovski I; Djuric O; Caraffi SG; Errichiello E; Marinelli M; Franchi F; Bizzarri V; Rosato S; Pollazzon M; Gelmini C; Malacarne M; Fusco C; Gargano G; Bernasconi S; Zuffardi O; Garavelli L
    Ital J Pediatr; 2018 Mar; 44(1):34. PubMed ID: 29523172
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual Disability.
    Türkyılmaz A; Geckinli BB; Tekin E; Ates EA; Yarali O; Cebi AH; Arman A
    Balkan J Med Genet; 2021 Nov; 24(2):15-24. PubMed ID: 36249514
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
    D'Amours G; Langlois M; Mathonnet G; Fetni R; Nizard S; Srour M; Tihy F; Phillips MS; Michaud JL; Lemyre E
    BMC Med Genomics; 2014 Dec; 7():70. PubMed ID: 25539807
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Application of chromosomal microarrays in the evaluation of intellectual disability/global developmental delay patients - A study from a tertiary care genetic centre in India.
    Sharma P; Gupta N; Chowdhury MR; Sapra S; Ghosh M; Gulati S; Kabra M
    Gene; 2016 Sep; 590(1):109-19. PubMed ID: 27291820
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients.
    Choucair N; Ghoch JA; Corbani S; Cacciagli P; Mignon-Ravix C; Salem N; Jalkh N; El Sabbagh S; Fawaz A; Ibrahim T; Villard L; Mégarbané A; Chouery E
    Mol Cytogenet; 2015; 8():26. PubMed ID: 25922617
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes.
    Correa FA; Jorge AA; Nakaguma M; Canton AP; Costa SS; Funari MF; Lerario AM; Franca MM; Carvalho LR; Krepischi AC; Arnhold IJ; Rosenberg C; Mendonca BB
    Clin Endocrinol (Oxf); 2018 Mar; 88(3):425-431. PubMed ID: 29265571
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Considering specific clinical features as evidence of pathogenic copy number variants.
    Preiksaitiene E; Molytė A; Kasnauskiene J; Ciuladaite Z; Utkus A; Patsalis PC; Kučinskas V
    J Appl Genet; 2014 May; 55(2):189-96. PubMed ID: 24535828
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Assessment of copy number variations in 120 patients with Poland syndrome.
    Vaccari CM; Tassano E; Torre M; Gimelli S; Divizia MT; Romanini MV; Bossi S; Musante I; Valle M; Senes F; Catena N; Bedeschi MF; Baban A; Calevo MG; Acquaviva M; Lerone M; Ravazzolo R; Puliti A
    BMC Med Genet; 2016 Nov; 17(1):89. PubMed ID: 27884122
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.