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 *

992 related articles for article (PubMed ID: 31337399)

  • 1. 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]  

  • 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. 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]  

  • 4. The usefulness of array comparative genomic hybridization in clinical diagnostics of intellectual disability in children.
    Bartnik M; Wiśniowiecka-Kowalnik B; Nowakowska B; Smyk M; Kędzior M; Sobecka K; Kutkowska-Kaźmierczak A; Klapecki J; Szczałuba K; Castañeda J; Własienko P; Bezniakow N; Obersztyn E; Bocian E
    Dev Period Med; 2014; 18(3):307-17. PubMed ID: 25182394
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Molecular diagnosis of children with unexplained intellectual disability/ developmental delay by array-CGH].
    He XY; Chen XC; Li R; Li P; Lu AM
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 May; 17(5):459-63. PubMed ID: 26014695
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.
    Nicholl J; Waters W; Mulley JC; Suwalski S; Brown S; Hull Y; Barnett C; Haan E; Thompson EM; Liebelt J; Mcgregor L; Harbord MG; Entwistle J; Munt C; White D; Chitti A; Baulderstone D; Ketteridge D; ; Friend K; Bain SM; Yu S
    Pathology; 2014 Jan; 46(1):41-5. PubMed ID: 24300712
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Array CGH analysis of a cohort of Russian patients with intellectual disability.
    Kashevarova AA; Nazarenko LP; Skryabin NA; Salyukova OA; Chechetkina NN; Tolmacheva EN; Sazhenova EA; Magini P; Graziano C; Romeo G; Kučinskas V; Lebedev IN
    Gene; 2014 Feb; 536(1):145-50. PubMed ID: 24291026
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [The diagnostic value of chromosome microarray analysis technique in the genetic causes of children with intellectual disability or global developmental delay].
    Wu HR; Li L; Ma YN; Liu CL; Pei P; Zheng XF; Wang ST; Xiao Y; Bu DF; Xu YF; Pan H; Qi Y
    Zhonghua Yi Xue Za Zhi; 2021 Jan; 101(3):224-228. PubMed ID: 33455150
    [No Abstract]   [Full Text] [Related]  

  • 13. Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders.
    Bartnik M; Szczepanik E; Derwińska K; Wiśniowiecka-Kowalnik B; Gambin T; Sykulski M; Ziemkiewicz K; Kędzior M; Gos M; Hoffman-Zacharska D; Mazurczak T; Jeziorek A; Antczak-Marach D; Rudzka-Dybała M; Mazurkiewicz H; Goszczańska-Ciuchta A; Zalewska-Miszkurka Z; Terczyńska I; Sobierajewicz M; Shaw CA; Gambin A; Mierzewska H; Mazurczak T; Obersztyn E; Bocian E; Stankiewicz P
    Am J Med Genet B Neuropsychiatr Genet; 2012 Oct; 159B(7):760-71. PubMed ID: 22825934
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Routine chromosomal microarray analysis is necessary in Korean patients with unexplained developmental delay/mental retardation/autism spectrum disorder.
    Shin S; Yu N; Choi JR; Jeong S; Lee KA
    Ann Lab Med; 2015 Sep; 35(5):510-8. PubMed ID: 26206688
    [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. Recurrent benign copy number variants & issues in interpretation of variants of unknown significance identified by cytogenetic microarray in Indian patients with intellectual disability.
    Boggula VR; Agarwal M; Kumar R; Awasthi S; Phadke SR
    Indian J Med Res; 2015 Dec; 142(6):699-712. PubMed ID: 26831419
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Array-CGH analysis in patients with intellectual disability and/or congenital malformations in Brazil.
    Vianna GS; Medeiros PF; Alves AF; Silva TO; Jehee FS
    Genet Mol Res; 2016 Feb; 15(1):. PubMed ID: 26909975
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability.
    Bartnik M; Nowakowska B; Derwińska K; Wiśniowiecka-Kowalnik B; Kędzior M; Bernaciak J; Ziemkiewicz K; Gambin T; Sykulski M; Bezniakow N; Korniszewski L; Kutkowska-Kaźmierczak A; Klapecki J; Szczałuba K; Shaw CA; Mazurczak T; Gambin A; Obersztyn E; Bocian E; Stankiewicz P
    J Appl Genet; 2014 Feb; 55(1):125-44. PubMed ID: 24297458
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 50.