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 *

74 related articles for article (PubMed ID: 30703237)

  • 1. [Genome-wide copy number microarray analysis for a boy with autism].
    He X; Zhao P; Huang Y; Cai X; Bi B; Lin J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Feb; 36(2):157-160. PubMed ID: 30703237
    [TBL] [Abstract][Full Text] [Related]  

  • 2. High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families.
    AlAyadhi LY; Hashmi JA; Iqbal M; Albalawi AM; Samman MI; Elamin NE; Bashir S; Basit S
    Neuroscience; 2016 Dec; 339():561-570. PubMed ID: 27771533
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis.
    Griswold AJ; Ma D; Sacharow SJ; Robinson JL; Jaworski JM; Wright HH; Abramson RK; Lybaek H; Øyen N; Cuccaro ML; Gilbert JR; Pericak-Vance MA
    Autism Res; 2011 Jun; 4(3):221-7. PubMed ID: 21360829
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
    Weiss LA
    Expert Rev Mol Diagn; 2009 Nov; 9(8):795-803. PubMed ID: 19895225
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Chromosome microarray analysis of patients with 18q deletion syndrome].
    Feng J; Hao J; Chen Y; Li F; Han J; Li R; Zhang Y; Lei T; Chen F; Guo Q; Liao C; Wang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):203-7. PubMed ID: 27060316
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genome-wide copy number profiling using a 100K SNP array reveals novel disease-related genes BORIS and TSHZ1 in juvenile angiofibroma.
    Schick B; Wemmert S; Willnecker V; Dlugaiczyk J; Nicolai P; Siwiec H; Thiel CT; Rauch A; Wendler O
    Int J Oncol; 2011 Nov; 39(5):1143-51. PubMed ID: 21874228
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Phenotypic and genotypic analysis of a girl carrying a 2q22.3 microduplication encompassing the MBD5 gene].
    He X; Huang Y; Luo S; Cai X; Zeng C; Lin J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Jun; 36(6):624-627. PubMed ID: 31055822
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Saliva DNA: An alternative biospecimen for single nucleotide polymorphism chromosomal microarray analysis in autism.
    Wright DC; Baluyot ML; Carmichael J; Darmanian A; Jose N; Ngo C; Heaps LS; Yendle A; Holman K; Ziso S; Khan F; Masi A; Silove N; Eapen V
    Am J Med Genet A; 2023 Dec; 191(12):2913-2920. PubMed ID: 37715344
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Genotype and phenotype analysis of a child with partial 18q deletion syndrome].
    Shi S; Guo L; Zha Q; Shi Z; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):567-570. PubMed ID: 28777861
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome-Wide Array Analysis Reveals Novel Genomic Regions and Candidate Gene for Intellectual Disability.
    Chen X; Li H; Chen C; Zhou L; Xu X; Xiang Y; Tang S
    Mol Diagn Ther; 2018 Dec; 22(6):749-757. PubMed ID: 30259421
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide identification of copy number variations in Holstein cattle from Baja California, Mexico, using high-density SNP genotyping arrays.
    Salomón-Torres R; González-Vizcarra VM; Medina-Basulto GE; Montaño-Gómez MF; Mahadevan P; Yaurima-Basaldúa VH; Villa-Angulo C; Villa-Angulo R
    Genet Mol Res; 2015 Oct; 14(4):11848-59. PubMed ID: 26436509
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.
    Cho SC; Yim SH; Yoo HK; Kim MY; Jung GY; Shin GW; Kim BN; Hwang JW; Kang JJ; Kim TM; Chung YJ
    Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Copy number variations in testicular maturation arrest.
    Halder A; Kumar P; Jain M; Iyer VK
    Andrology; 2017 May; 5(3):460-472. PubMed ID: 28217965
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
    Saadati HR; Wittig M; Helbig I; Häsler R; Anderson CA; Mathew CG; Kupcinskas L; Parkes M; Karlsen TH; Rosenstiel P; Schreiber S; Franke A
    BMC Med Genet; 2016 Apr; 17():26. PubMed ID: 27037036
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Application of single nucleotide polymorphism array for the identification of pathogenic copy number variations in fetuses with malformations and women with an adverse reproductive history].
    Liu J; Xi H; Wang H; Jia Z; Zhou Y; Wu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):173-177. PubMed ID: 28397212
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
    D'Amours G; Langlois M; Mathonnet G; Fetni R; Nizard S; Srour M; Tihy F; Phillips MS; Michaud JL; Lemyre E
    BMC Med Genomics; 2014 Dec; 7():70. PubMed ID: 25539807
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection and characterization of copy number variation in autism spectrum disorder.
    Marshall CR; Scherer SW
    Methods Mol Biol; 2012; 838():115-35. PubMed ID: 22228009
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability.
    Qiao Y; Tyson C; Hrynchak M; Lopez-Rangel E; Hildebrand J; Martell S; Fawcett C; Kasmara L; Calli K; Harvard C; Liu X; Holden JJ; Lewis SM; Rajcan-Separovic E
    Clin Genet; 2013 Feb; 83(2):145-54. PubMed ID: 22369279
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Structural variations of the genome in autistic spectrum disorders with intellectual disability].
    Iourov IY; Vorsanova SG; Korostelev SA; Vasin KS; Zelenova MA; Kurinnaia OS; Yurov YB
    Zh Nevrol Psikhiatr Im S S Korsakova; 2016; 116(7):50-54. PubMed ID: 27500877
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
    Borlot F; Regan BM; Bassett AS; Stavropoulos DJ; Andrade DM
    JAMA Neurol; 2017 Nov; 74(11):1301-1311. PubMed ID: 28846756
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.