BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

280 related articles for article (PubMed ID: 29196358)

  • 1. A clinical approach to developmental delay and intellectual disability.
    Vasudevan P; Suri M
    Clin Med (Lond); 2017 Dec; 17(6):558-561. PubMed ID: 29196358
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosomal Microarray With Clinical Diagnostic Utility in Children With Developmental Delay or Intellectual Disability.
    Lee JS; Hwang H; Kim SY; Kim KJ; Choi JS; Woo MJ; Choi YM; Jun JK; Lim BC; Chae JH
    Ann Lab Med; 2018 Sep; 38(5):473-480. PubMed ID: 29797819
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
    Battaglia A; Doccini V; Bernardini L; Novelli A; Loddo S; Capalbo A; Filippi T; Carey JC
    Eur J Paediatr Neurol; 2013 Nov; 17(6):589-99. PubMed ID: 23711909
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetics and the investigation of developmental delay/intellectual disability.
    Srour M; Shevell M
    Arch Dis Child; 2014 Apr; 99(4):386-9. PubMed ID: 24344174
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Testing scenario for intellectual disability, developmental delay, and autism challenged.
    Am J Med Genet A; 2018 Jan; 176(1):7-8. PubMed ID: 29232062
    [No Abstract]   [Full Text] [Related]  

  • 6. The prevalence of chromosomal deletions relating to developmental delay and/or intellectual disability in human euploid blastocysts.
    He W; Sun X; Liu L; Li M; Jin H; Wang WH
    PLoS One; 2014; 9(1):e85207. PubMed ID: 24409323
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability.
    Miclea D; Osan S; Bucerzan S; Stefan D; Popp R; Mager M; Puiu M; Zimbru C; Chirita-Emandi A; Alkhzouz C
    Ital J Pediatr; 2022 Dec; 48(1):207. PubMed ID: 36585697
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosomal Microarray Analysis Has a Poor Diagnostic Yield in Children with Developmental Delay/Intellectual Disability When Concurrent Cerebellar Anomalies Are Present.
    Ciaccio C; Pantaleoni C; Bulgheroni S; Sciacca F; D'Arrigo S
    Cerebellum; 2020 Oct; 19(5):629-635. PubMed ID: 32472476
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cost Effectiveness of Karyotyping, Chromosomal Microarray Analysis, and Targeted Next-Generation Sequencing of Patients with Unexplained Global Developmental Delay or Intellectual Disability.
    Li Y; Anderson LA; Ginns EI; Devlin JJ
    Mol Diagn Ther; 2018 Feb; 22(1):129-138. PubMed ID: 29209992
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic Analysis of Korean Patients with Abnormal Chromosomal Microarray in Patients with Unexplained Developmental Delay/Intellectual Disability.
    Kim HJ; Park CI; Lim JW; Lee GM; Cho E; Kim HJ
    Yonsei Med J; 2018 May; 59(3):431-437. PubMed ID: 29611406
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Diagnostic Yield of Array Comparative Genomic Hybridization Is High Regardless of Severity of Intellectual Disability/Developmental Delay in Children.
    D'Arrigo S; Gavazzi F; Alfei E; Zuffardi O; Montomoli C; Corso B; Buzzi E; Sciacca FL; Bulgheroni S; Riva D; Pantaleoni C
    J Child Neurol; 2016 May; 31(6):691-9. PubMed ID: 26511719
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenotype comparison among individuals with developmental delay/intellectual disability with or without genomic imbalances.
    de Souza LC; Dos Santos AP; Sgardioli IC; Viguetti-Campos NL; Marques Prota JR; de Oliveira-Sobrinho RP; Vieira TP; Gil-da-Silva-Lopes VL
    J Intellect Disabil Res; 2019 Nov; 63(11):1379-1389. PubMed ID: 30900361
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis.
    Prasad A; Sdano MA; Vanzo RJ; Mowery-Rushton PA; Serrano MA; Hensel CH; Wassman ER
    BMC Med Genet; 2018 Mar; 19(1):46. PubMed ID: 29554876
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Multiplex Ligation - dependent Probe Amplification (MLPA) as a screening test in children with developmental defects and intellectual disability of unknown etiology].
    Laczmańska I; Jakubiak A; Slęzak R; Pesz K; Stembalska A; Laczmański L; Sąsiadek MM; Smigiel R
    Med Wieku Rozwoj; 2011; 15(2):132-9. PubMed ID: 22002044
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotype.
    Kolarova J; Tangen I; Bens S; Gillessen-Kaesbach G; Gutwein J; Kautza M; Rydzanicz M; Stephani U; Siebert R; Ammerpohl O; Caliebe A
    Eur J Med Genet; 2015 Aug; 58(8):419-25. PubMed ID: 26003415
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Diagnostic approach with genetic tests for global developmental delay and/or intellectual disability: Single tertiary center experience.
    Han JY; Jang W; Park J; Kim M; Kim Y; Lee IG
    Ann Hum Genet; 2019 May; 83(3):115-123. PubMed ID: 30402882
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Comprehensive evaluation of the child with intellectual disability or global developmental delays.
    Moeschler JB; Shevell M;
    Pediatrics; 2014 Sep; 134(3):e903-18. PubMed ID: 25157020
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Utility of Chromosomal Microarray in Children with Unexplained Developmental Delay/Intellectual Disability.
    Kamath V; Yoganathan S; Thomas MM; Gowri M; Chacko MP
    Fetal Pediatr Pathol; 2022 Apr; 41(2):208-218. PubMed ID: 32701375
    [No Abstract]   [Full Text] [Related]  

  • 19. Exonic deletions of AUTS2 in Chinese patients with developmental delay and intellectual disability.
    Fan Y; Qiu W; Wang L; Gu X; Yu Y
    Am J Med Genet A; 2016 Feb; 170A(2):515-522. PubMed ID: 26545289
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 14.