BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 34604135)

  • 21. 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]  

  • 22. Performance of chromosomal microarray for patients with intellectual disabilities/developmental delay, autism, and multiple congenital anomalies in a Chinese cohort.
    Chong WW; Lo IF; Lam ST; Wang CC; Luk HM; Leung TY; Choy KW
    Mol Cytogenet; 2014; 7():34. PubMed ID: 24926319
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Chromosome microarray analysis in the investigation of children with congenital heart disease.
    Wu XL; Li R; Fu F; Pan M; Han J; Yang X; Zhang YL; Li FT; Liao C
    BMC Pediatr; 2017 May; 17(1):117. PubMed ID: 28472932
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinical utility and cost-effectiveness analysis of chromosome testing concomitant with chromosomal microarray of patients with constitutional disorders in a U.S. academic medical center.
    Su M; Page S; Haag M; Swisshelm K; Hennerich D; Graw S; LeRoux J; Brzeskiewicz P; Svihovec S; Bao L
    J Genet Couns; 2022 Apr; 31(2):364-374. PubMed ID: 34397147
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong.
    Cheng SSW; Chan KYK; Leung KKP; Au PKC; Tam WK; Li SKM; Luk HM; Kan ASY; Chung BHY; Lo IFM; Tang MHY
    Am J Med Genet C Semin Med Genet; 2019 Jun; 181(2):196-207. PubMed ID: 30903683
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability-Data from a Romanian Cohort.
    Streață I; Caramizaru A; Riza AL; Șerban-Sosoi S; Pîrvu A; Cara ML; Cucu MG; Dobrescu AM; Ro-Nmca-Id Group ; CExBR Pediatric Neurology Obregia Group ; CExBR Pediatric Neurology V Gomoiu Hospital Group ; Shelby ES; Albeanu A; Burada F; Ioana M
    Diagnostics (Basel); 2022 Dec; 12(12):. PubMed ID: 36553144
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Comparative Benchmarking of Optical Genome Mapping and Chromosomal Microarray Reveals High Technological Concordance in CNV Identification and Additional Structural Variant Refinement.
    Barseghyan H; Pang AWC; Clifford B; Serrano MA; Chaubey A; Hastie AR
    Genes (Basel); 2023 Sep; 14(10):. PubMed ID: 37895217
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders.
    Gürkan H; Atli Eİ; Atli E; Bozatli L; Altay MA; Yalçintepe S; Özen Y; Eker D; Akurut Ç; Demır S; Görker I
    Noro Psikiyatr Ars; 2020 Sep; 57(3):177-191. PubMed ID: 32952419
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [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]  

  • 35. CNV profiles of Chinese pediatric patients with developmental disorders.
    Yuan H; Shangguan S; Li Z; Luo J; Su J; Yao R; Zhang S; Liang C; Chen Q; Gao Z; Zhu Y; Zhang S; Li W; Lu W; Zhang Y; Xie H; Liu F; Wang Q; Lin Y; Liu L; Wang X; Liang L; Zhong J; Li H; Qiu H; Zhang H; Yan M; Mireguli M; Liu Y; Zhang D; Wang H; Lv H; Xie B; Gui C; Cui X; Zou L; Wang J; Gusella JF; Shen Y; Chen X
    Genet Med; 2021 Apr; 23(4):669-678. PubMed ID: 33402738
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Additive Diagnostic Yield of Homozygosity Regions Identified During Chromosomal microarray Testing in Children with Developmental Delay, Dysmorphic Features or Congenital Anomalies.
    Ali MAM; Hassan AM; Saafan MA; Abdelmagid AA
    Biochem Genet; 2020 Feb; 58(1):74-101. PubMed ID: 31273557
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. [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]  

  • 40. MLPA is a practical and complementary alternative to CMA for diagnostic testing in patients with autism spectrum disorders and identifying new candidate CNVs associated with autism.
    Capkova P; Srovnal J; Capkova Z; Staffova K; Becvarova V; Trkova M; Adamova K; Santava A; Curtisova V; Hajduch M; Prochazka M
    PeerJ; 2019; 6():e6183. PubMed ID: 30647996
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.