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: 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. [Genetic analysis of a fetus with with 45,X/46,X,idic(Y)(q11.2) mosaicism].
    Pan F; Zhang W; Zhang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Aug; 41(8):897-902. PubMed ID: 39097269
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. [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]  

  • 9. 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]  

  • 10. [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]  

  • 11. [Comprehensive diagnosis and genetic analysis of two children with ring chromosome 18].
    Ding Z; Mei S; Zhang B; Kong J; Liu L; Zhang Z; Wang C; Zhang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Sep; 41(9):1110-1116. PubMed ID: 39217492
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. [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]  

  • 14. 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]  

  • 15. 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]  

  • 16. [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]  

  • 17. 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]  

  • 18. 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]  

  • 19. [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]  

  • 20. [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]  

    [Next]    [New Search]
    of 7.