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 *

182 related articles for article (PubMed ID: 36854406)

  • 1. [Application of copy number variation sequencing in patients with intellectual disability/developmental delay and autistic spectrum disorder].
    Lei J; Zhao G; Huang Y; Long M; Li W; Deng X; Xiu Z; Xiao Y; Zeng S; Zhang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Mar; 40(3):308-316. PubMed ID: 36854406
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. [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]  

  • 5. [Value of copy number variation analysis and chromosomal karyotyping for the diagnosis of children with intellectual disability/developmental delay].
    Lin M; Xue H; Wang Y; Huang H; Fu M; Guo N; Xu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):228-231. PubMed ID: 33751530
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. High-resolution chromosomal microarray analysis for copy-number variations in high-functioning autism reveals large aberration typical for intellectual disability.
    Werling AM; Grünblatt E; Oneda B; Bobrowski E; Gundelfinger R; Taurines R; Romanos M; Rauch A; Walitza S
    J Neural Transm (Vienna); 2020 Jan; 127(1):81-94. PubMed ID: 31838600
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Application of single nucleotide polymorphism-microarray and target gene sequencing in the study of genetic etiology of children with unexplained intellectual disability or developmental delay].
    Gao ZJ; Jiang Q; Cheng DZ; Yan XX; Chen Q; Xu KM
    Zhonghua Er Ke Za Zhi; 2016 Oct; 54(10):740-745. PubMed ID: 27784475
    [No Abstract]   [Full Text] [Related]  

  • 11. [Detection of genomic copy number variations in patients with unexplained mental retardation/developmental delay by low coverage whole-genome sequencing].
    Song H; Shi P; Xiao Y; Hou Y; Chen D; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):953-957. PubMed ID: 32820506
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders From the South of Brazil.
    Chaves TF; Baretto N; Oliveira LF; Ocampos M; Barbato IT; Anselmi M; De Luca GR; Barbato Filho JH; Pinto LLC; Bernardi P; Maris AF
    Sci Rep; 2019 Nov; 9(1):17776. PubMed ID: 31780800
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. [Application of chromosome microarray analysis in 489 children with developmental delay/intellectual disability].
    Wang R; Lei T; Fu F; Li R; Jing X; Yang X; Pan M; Li D; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):528-533. PubMed ID: 28777852
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An ethical analysis of divergent clinical approaches to the application of genetic testing for autism and schizophrenia.
    Morris E; O'Donovan M; Virani A; Austin J
    Hum Genet; 2022 May; 141(5):1069-1084. PubMed ID: 34453583
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.