BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 24535828)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China.
    Wang R; Lei T; Fu F; Li R; Jing X; Yang X; Liu J; Li D; Liao C
    Pediatr Neonatol; 2019 Feb; 60(1):35-42. PubMed ID: 29631977
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Chromosomal Aberrations in Pediatric Patients with Developmental Delay/Intellectual Disability: A Single-Center Clinical Investigation.
    Hu T; Zhang Z; Wang J; Li Q; Zhu H; Lai Y; Wang H; Liu S
    Biomed Res Int; 2019; 2019():9352581. PubMed ID: 31781653
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
    Shoukier M; Klein N; Auber B; Wickert J; Schröder J; Zoll B; Burfeind P; Bartels I; Alsat EA; Lingen M; Grzmil P; Schulze S; Keyser J; Weise D; Borchers M; Hobbiebrunken E; Röbl M; Gärtner J; Brockmann K; Zirn B
    Clin Genet; 2013 Jan; 83(1):53-65. PubMed ID: 22283495
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes.
    Di Gregorio E; Riberi E; Belligni EF; Biamino E; Spielmann M; Ala U; Calcia A; Bagnasco I; Carli D; Gai G; Giordano M; Guala A; Keller R; Mandrile G; Arduino C; Maffè A; Naretto VG; Sirchia F; Sorasio L; Ungari S; Zonta A; Zacchetti G; Talarico F; Pappi P; Cavalieri S; Giorgio E; Mancini C; Ferrero M; Brussino A; Savin E; Gandione M; Pelle A; Giachino DF; De Marchi M; Restagno G; Provero P; Cirillo Silengo M; Grosso E; Buxbaum JD; Pasini B; De Rubeis S; Brusco A; Ferrero GB
    Clin Genet; 2017 Oct; 92(4):415-422. PubMed ID: 28295210
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnostic yield of the chromosomal microarray analysis in turkish patients with unexplained development delay/ıntellectual disability(ID), autism spectrum disorders and/or multiple congenital anomalies and new clinical findings.
    Akkus N; Cubuk PO
    Mol Biol Rep; 2024 Apr; 51(1):577. PubMed ID: 38664339
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 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. 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]  

  • 16. 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]  

  • 17. Genomic study via chromosomal microarray analysis in a group of Romanian patients with obesity and developmental disability/intellectual disability.
    Micleaa D; Al-Khzouza C; Osan S; Bucerzan S; Cret V; Popp RA; Puiu M; Chirita-Emandi A; Zimbru C; Ghervan C
    J Pediatr Endocrinol Metab; 2019 Jul; 32(7):667-674. PubMed ID: 31150357
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Predictive diagnostic value for the clinical features accompanying intellectual disability in children with pathogenic copy number variations: a multivariate analysis.
    Caramaschi E; Stanghellini I; Magini P; Giuffrida MG; Scullin S; Giuva T; Bergonzini P; Guerra A; Paolucci P; Percesepe A
    Ital J Pediatr; 2014 Apr; 40():39. PubMed ID: 24775911
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions.
    Fan Y; Wu Y; Wang L; Wang Y; Gong Z; Qiu W; Wang J; Zhang H; Ji X; Ye J; Han L; Jin X; Shen Y; Li F; Xiao B; Liang L; Zhang X; Liu X; Gu X; Yu Y
    BMC Med Genomics; 2018 May; 11(1):49. PubMed ID: 29793483
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.