BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 36709940)

  • 1. [Application of low-depth whole genome sequencing for copy number variation analysis in children with disorders of sex development].
    Xia J; Hou Y; Dai P; Zhao Z; Chen C; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Feb; 40(2):195-201. PubMed ID: 36709940
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Clinical and genetic characteristic in patients with disorders of sex development caused by Y chromosome copy number variant].
    Xia JK; Tian FY; Hou YQ; Zhao YJ; Kong XD
    Zhonghua Er Ke Za Zhi; 2023 May; 61(5):459-463. PubMed ID: 37096267
    [No Abstract]   [Full Text] [Related]  

  • 3. [Genetic analysis of a rare case with Disorder of sex development due to structural rearrangement of Y chromosome].
    Mi M; Xia J; Hou Y; Dai P; Wang Y; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Nov; 40(11):1430-1435. PubMed ID: 37906155
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal genetic testing in 19 fetuses with corpus callosum abnormality.
    She Q; Tang E; Peng C; Wang L; Wang D; Tan W
    J Clin Lab Anal; 2021 Nov; 35(11):e23971. PubMed ID: 34569664
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.
    Liu S; Song L; Cram DS; Xiong L; Wang K; Wu R; Liu J; Deng K; Jia B; Zhong M; Yang F
    Ultrasound Obstet Gynecol; 2015 Oct; 46(4):472-7. PubMed ID: 25767059
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Combined use of karyotyping and copy number variation sequencing technology in prenatal diagnosis.
    Zhang S; Xu Y; Lu D; Fu D; Zhao Y
    PeerJ; 2022; 10():e14400. PubMed ID: 36523456
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with congenital gastrointestinal obstruction.
    Meng X; Jiang L
    BMC Pregnancy Childbirth; 2022 Jan; 22(1):50. PubMed ID: 35045821
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Prenatal diagnosis for two fetuses carrying partial deletion of Y chromosome].
    Pang H; Gao M; Hua J; Tong D; Zhao Y; Feng X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Feb; 37(2):182-185. PubMed ID: 32034751
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Diagnosis of a case of 2q37 deletion syndrome by whole exome sequencing combined with whole genome low-coverage sequencing method].
    Lin H; Bai L; Yue Y; Xi X; Chen W; Zhou C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Aug; 37(8):883-886. PubMed ID: 32761601
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Genetic analysis of three children with disorders of sex development caused by structural rearrangements of Y chromosome].
    Wang H; Chen L; Chen Y; Shen Y; Li L; Shao X; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1226-1232. PubMed ID: 33179226
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Efficacy of copy-number variation sequencing technology in prenatal diagnosis.
    Zhao X; Fu L
    J Perinat Med; 2019 Aug; 47(6):651-655. PubMed ID: 31287799
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis.
    Zhang J; Tang X; Hu J; He G; Wang J; Zhu Y; Zhu B
    BMC Pregnancy Childbirth; 2021 Jul; 21(1):496. PubMed ID: 34238233
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [SRY gene-testing in the diagnosis of disorders of sex development among children].
    Xiang PX; Dai X; Leng P; Liu L; Hu XJ
    Zhongguo Dang Dai Er Ke Za Zhi; 2013 Jul; 15(7):555-8. PubMed ID: 23866278
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Additional diagnostic value of CNV-seq over conventional karyotyping in prenatal diagnosis: A systematic review and meta-analysis.
    Luo H; Wang Q; Fu D; Gao J; Lu D
    J Obstet Gynaecol Res; 2023 Jul; 49(7):1641-1650. PubMed ID: 37037422
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Copy number variations (CNVs) and karyotyping analysis in males with azoospermia and oligospermia.
    Xin X; Xu P; Wang N; Jiang Y; Zhang J; Li S; Zhu Y; Zhang C; Zhang L; Huang H; Feng L; Wang S
    BMC Med Genomics; 2023 Sep; 16(1):213. PubMed ID: 37684669
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Application value of CNV-seq for the prenatal diagnosis of women with high-risk pregnancies].
    Xiang P; Liu L; Hu X; Zhou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jan; 40(1):17-20. PubMed ID: 36584994
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Application of CNV-seq and chromosomal karyotyping in the prenatal diagnosis for carriers of balanced translocations].
    Qu S; Shi P; Zhang T; Gao Z; Guan H; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Apr; 39(4):366-369. PubMed ID: 35446967
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical characteristics, cytogenetic and molecular findings in patients with disorders of sex development.
    Tian L; Chen M; Peng JH; Zhang JW; Li L
    J Huazhong Univ Sci Technolog Med Sci; 2014 Feb; 34(1):81-86. PubMed ID: 24496683
    [TBL] [Abstract][Full Text] [Related]  

  • 20. New insights from unbiased panel and whole-exome sequencing in a large Chinese cohort with disorders of sex development.
    Xu Y; Wang Y; Li N; Yao R; Li G; Li J; Ding Y; Chen Y; Huang X; Chen Y; Qing Y; Yu T; Shen Y; Wang X; Shen Y; Wang J
    Eur J Endocrinol; 2019 Sep; 181(3):311-323. PubMed ID: 31277073
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.