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 *

127 related articles for article (PubMed ID: 32034736)

  • 1. [Genetic analysis of a child with Sotos syndrome].
    Luo Y; Sun Y; Qian Y; Shen M; Wang L; Jin F; Dong M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Feb; 37(2):127-130. PubMed ID: 32034736
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Genetic analysis of a child with mental retardation and hypospadia].
    Ma N; Pang J; Peng Y; Jia Z; Xi H; Liu G; Zhou Y; Wang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec; 36(12):1199-1202. PubMed ID: 31813147
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Genetic diagnosis of a fetus with Dandy-Walker syndrome].
    Luo Y; Sun Y; Qian Y; Shen M; Wang L; Jin F; Dong M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jan; 37(1):8-11. PubMed ID: 31922586
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Clinical features and genetic analysis of two cases with 16p13.3 microdeletion and 19q13.4 microduplication derived from familial cryptic balanced translocation].
    Xu H; Ji X; Ni L; Zhu Y; Chen Y; Xiao B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug; 33(4):490-3. PubMed ID: 27455004
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Prenatal diagnosis of 1p36.3 microdeletion in a fetus with complex heart defect].
    Wu J; He Z; Lin S; Xie Y; Chen B; Chen J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):353-6. PubMed ID: 27264820
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome.
    Chen CP; Lin CJ; Chern SR; Liu YP; Kuo YL; Chen YN; Wu PS; Town DD; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):583-7. PubMed ID: 25510705
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Molecular genetic analysis of a child with de novo 16p11.2 microdeletion].
    Zhuang J; Wang Y; Zeng S; Wang J; Jiang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1283-1286. PubMed ID: 33179241
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Prenatal genetic analysis of a fetus with Wolf-Hirschhorn syndrome and Edward syndrome].
    Shen X; He P; Fang R; Yao J; Li W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):714-717. PubMed ID: 28981940
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of a girl with Phelan-McDermid syndrome].
    Zhao L; Wan B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Feb; 36(2):154-156. PubMed ID: 30703236
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Xq;Yq translocation in a patient with premature ovarian insufficiency].
    Yang S; Zhang Y; Hu J; Hu R; Jia Z; Xi H; Wang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):942-945. PubMed ID: 32820504
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Diagnosis of a case with recurrent pregnancy loss resulted from maternal balanced translocation by chromosomal microarray analysis].
    Wang L; Bai N; Liu L; Zhang Q; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Jun; 35(3):443-447. PubMed ID: 29896752
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unbalanced der(5)t(5;20) translocation associated with megalencephaly, perisylvian polymicrogyria, polydactyly and hydrocephalus.
    Verkerk AJ; Schot R; van Waterschoot L; Douben H; Poddighe PJ; Lequin MH; de Vries LS; Terhal P; Hahnemann JM; de Coo IF; de Wit MC; Wafelman LS; Garavelli L; Dobyns WB; Van der Spek PJ; de Klein A; Mancini GM
    Am J Med Genet A; 2010 Jun; 152A(6):1488-97. PubMed ID: 20503325
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Phenotypic and genetic analysis of a boy with a 10p15.3 deletion and partial trisomy 18p syndrome].
    Zhang B; Kong J; Mei S; Li D; Song Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):785-788. PubMed ID: 32619265
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A case of Wolf-Hirschhorn syndrome diagnosed by single nucleotide polymorphism array].
    Jin Y; Liu X; Li S; Zhou C; Liu X; Song Q; Wang L; Miao Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug; 33(4):501-4. PubMed ID: 27455007
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetic analysis of a fetus with multiple malformations caused by complex translocations of four chromosomes].
    Luo Y; Shen M; Sun Y; Qian Y; Wang L; Yu J; Hu J; Jin F; Dong M
    Zhejiang Da Xue Xue Bao Yi Xue Ban; 2019 Jun; 48(4):397-402. PubMed ID: 31901043
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genetic analysis of a fetus with partial 1q monosomy and partial 17q trisomy].
    Lin S; Zhang Z; Wu J; Ji Y; Fang Q; Chen B; Zhou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):340-3. PubMed ID: 27264817
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Prenatal diagnosis of a case of Pallister-Killian syndrome].
    Xi H; Wang H; Jia Z; Zhou Y; Yu H; Liu J; Wu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Feb; 32(1):73-6. PubMed ID: 25636105
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Diagnosis of a case with Williams-Beuren syndrome by single nucleotide polymorphism array].
    Jin Y; Liu X; Li S; Ge J; Wu X; Song Q; Zhou C; Miao Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Aug; 32(4):529-32. PubMed ID: 26252101
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Genetic analysis of a case with 2q37 microdeletion syndrome].
    Lian X; Zhang X; Huang M; Lin J; Zeng J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jan; 39(1):81-84. PubMed ID: 34964974
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genetic analysis of a child with XYY syndrome mainly featuring mental retardation].
    Liu Y; Dong R; Zhang K; Wang Y; Zhang H; Zhang Y; Zhao D; Gai Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):686-9. PubMed ID: 27577224
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.