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 *

163 related articles for article (PubMed ID: 34304418)

  • 1. [Explore the value of whole exome sequencing in early diagnosis for children with language delay/disorder].
    Wang JH; Xie H; Xu Q; Tian Y; Wang X; Shangguan SF; Zhang Y; Lu HY; Chen XL; Wang L
    Zhonghua Yu Fang Yi Xue Za Zhi; 2021 Jul; 55(7):827-834. PubMed ID: 34304418
    [No Abstract]   [Full Text] [Related]  

  • 2. [Analysis of neuropsychological development characteristics and influencing factors in children with speech sound disorder].
    Liu XL; Wang JH; Xu Q; Wang L; Zhou B; Zhang LL; Wang L
    Zhonghua Yu Fang Yi Xue Za Zhi; 2023 Mar; 57(3):356-361. PubMed ID: 36922170
    [No Abstract]   [Full Text] [Related]  

  • 3. [Diagnostic value of whole exome sequencing for patients with intellectual disability or global developmental delay].
    Li Y; Lei D; Li C; Huang D; Tan J; Zhang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jun; 40(6):648-654. PubMed ID: 37211997
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular findings in patients for whole exome sequencing and mitochondrial genome assessment.
    Sun G; Huang W; Wang L; Wu J; Zhao G; Ren H; Liu L; Kong X
    Clin Chim Acta; 2024 Jul; 561():119774. PubMed ID: 38852791
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Clinical and genetic analysis of three children with Menkes disease due to variants of ATP7A gene].
    Wang Z; Chen Q; Wang Y; Liu L; Li C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jun; 40(6):668-673. PubMed ID: 37212000
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Correlation of early neurodevelopmental features of children with SYNGAP1 variants and their genotypes].
    Liu H; Yang S; Li J; Xie H; Chen X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Jan; 41(1):25-31. PubMed ID: 38171555
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical Utility of Next-Generation Sequencing for Developmental Disorders in the Rehabilitation Department: Experiences from a Single Chinese Center.
    Liu Y; Liu X; Qin D; Zhao Y; Cao X; Deng X; Cheng Y; Liu F; Yang F; Zhang T; Yang XA
    J Mol Neurosci; 2021 Apr; 71(4):845-853. PubMed ID: 32959227
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Targeted sequencing and clinical strategies in children with autism spectrum disorder: A cohort study.
    Hu C; Wang Y; Li C; Mei L; Zhou B; Li D; Li H; Xu Q; Xu X
    Front Genet; 2023; 14():1083779. PubMed ID: 37007974
    [No Abstract]   [Full Text] [Related]  

  • 9. Whole-exome sequencing enables rapid and prenatal diagnosis of inherited skin disorders.
    Xintong Z; Kexin Z; Junwen W; Ziyi W; Na L; Hong G
    BMC Med Genomics; 2023 Aug; 16(1):193. PubMed ID: 37605172
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of Disease-Causing SNVs/Indels and CNVs in Single Test Based on Whole Exome Sequencing: A Retrospective Case Study in Epileptic Encephalopathies.
    Sun D; Liu Y; Cai W; Ma J; Ni K; Chen M; Wang C; Liu Y; Zhu Y; Liu Z; Zhu F
    Front Pediatr; 2021; 9():635703. PubMed ID: 34055682
    [No Abstract]   [Full Text] [Related]  

  • 11. [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]  

  • 12. [Study of
    Gao ZJ; Jiang Q; Chen XL; Chen Q; Ji XN; Mao YY; Feng S; Dong JJ; Xu KM
    Zhonghua Yi Xue Za Zhi; 2018 Nov; 98(42):3426-3432. PubMed ID: 30440138
    [No Abstract]   [Full Text] [Related]  

  • 13. [Analysis of language and influencing factors of children with speech disorder in Beijing].
    Wang JH; Xu Q; Duan HF; Wang L; Zhou B; Zhang LL; Wang X; Zhou LJ; Liu XM; Wang L
    Zhonghua Er Ke Za Zhi; 2024 May; 62(5):438-443. PubMed ID: 38623011
    [No Abstract]   [Full Text] [Related]  

  • 14. Identification of genetic causes in children with unexplained epilepsy based on trio-whole exome sequencing.
    Chengyan L; Chupeng X; You W; Yinhui C; Binglong H; Dang A; Ling L; Chuan T
    Clin Genet; 2024 Aug; 106(2):140-149. PubMed ID: 38468460
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparison of Genetic Profiles of Neonates in Intensive Care Units Conceived With or Without Assisted Reproductive Technology.
    Huang Z; Xiao F; Xiao H; Lu Y; Yang L; Zhuang D; Chen L; Wei Q; Jiang Y; Li G; Wu B; Liu Z; Zhou W; Wang H
    JAMA Netw Open; 2023 Apr; 6(4):e236537. PubMed ID: 37014641
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort.
    Dong X; Liu B; Yang L; Wang H; Wu B; Liu R; Chen H; Chen X; Yu S; Chen B; Wang S; Xu X; Zhou W; Lu Y
    J Med Genet; 2020 Aug; 57(8):558-566. PubMed ID: 32005694
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The combination of whole-exome sequencing and copy number variation sequencing enables the diagnosis of rare neurological disorders.
    Jiao Q; Sun H; Zhang H; Wang R; Li S; Sun D; Yang XA; Jin Y
    Clin Genet; 2019 Aug; 96(2):140-150. PubMed ID: 30945278
    [TBL] [Abstract][Full Text] [Related]  

  • 18. CNV analysis using whole exome sequencing identified biallelic CNVs of VPS13B in siblings with intellectual disability.
    Enomoto Y; Tsurusaki Y; Yokoi T; Abe-Hatano C; Ida K; Naruto T; Mitsui J; Tsuji S; Morishita S; Kurosawa K
    Eur J Med Genet; 2020 Jan; 63(1):103610. PubMed ID: 30602132
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.
    Qi Q; Jiang Y; Zhou X; Meng H; Hao N; Chang J; Bai J; Wang C; Wang M; Guo J; Ouyang Y; Xu Z; Xiao M; Zhang VW; Liu J
    Genes (Basel); 2020 Nov; 11(12):. PubMed ID: 33255631
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of the genetic basis of pediatric neurogenetic disorders at a tertiary referral hospital in Indonesia: Contribution of whole exome sequencing.
    Triono A; Iskandar K; Hadiyanto ML; Nugrahanto AP; Diantika K; Wijayanti VW; Herini ES
    PLoS One; 2023; 18(10):e0293113. PubMed ID: 37878632
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.