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 *

157 related articles for article (PubMed ID: 33974260)

  • 1. [Genetic analysis of a fetus with partial 18p deletion].
    Chen X; Zhu Y; Zhang W; Yan W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 May; 38(5):477-480. PubMed ID: 33974260
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Prenatal diagnosis of a fetus with chromosome 18p deletion and duplication].
    Li W; Shao H; Yao J; Shi C; Yang X; Zhang J; Zhang X; Shen G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Jun; 38(6):569-572. PubMed ID: 34096028
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Prenatal genetic diagnosis of a case with ring chromosome 13].
    Sun L; Wen J; Chu G; Lai G; He R
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Dec; 40(12):1455-1460. PubMed ID: 37994123
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Prenatal diagnosis and genetic analysis of a 46,XN,del(11)(q14q22) fetus].
    Zhao L; Luo H; Luo G; Qiu X; Liao Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Aug; 37(8):879-882. PubMed ID: 32761600
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Accidental discovery of copy number variation on chromosome 1 in a fetus with high risk of trisomy 13 suggested by NIPT].
    Chang J; Song Y; Qi Q; Hao N; Liu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):922-927. PubMed ID: 37532489
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal detection of distal 18p deletion by chromosomal microarray analysis: Three case reports and literature review.
    Xu T; Yue F; He J; Zhang H; Liu R
    Medicine (Baltimore); 2024 Jul; 103(30):e39046. PubMed ID: 39058883
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The genotype and phenotype of chromosome 18p deletion syndrome: Case series.
    Jin Q; Qiang R; Cai B; Wang X; Cai N; Zhen S; Zhai W
    Medicine (Baltimore); 2021 May; 100(18):e25777. PubMed ID: 33950970
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Genetic analysis of a fetus with de novo 46,X,der(X)t(X;Y)(q26;q11)].
    Wang Y; Zhang R; Yin T; Wang Z; Zheng A; Wang L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 May; 40(5):593-597. PubMed ID: 37102296
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. [Prenatal diagnosis of a fetus with 1p36 deletion syndrome and 3p26.3p25.2 duplication].
    Zhao J; Gao J; Zhao X; Li L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):617-621. PubMed ID: 38684312
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Prenatal diagnosis of a fetus with 46,XX (SRY positive) male syndrome].
    Shi D; Zhang Y; Zhou Y; Mao Q; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):1039-1042. PubMed ID: 32820526
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant woman.
    Zhu J; Qi H; Cao S; Cai L; Wen X; Tang G; Wan Q; Chen C; Wang J; Zeng W; Luo Y
    Mol Genet Genomic Med; 2019 Sep; 7(9):e868. PubMed ID: 31317671
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Prenatal diagnosis of two fetuses with Xp22.31 microdeletion syndrome indicated by non-invasive prenatal testing].
    Wang R; Xi M; Wei Y; Wei L; Zhu W; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):928-932. PubMed ID: 37532490
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic Analysis of 1p36 Deletions for Six Aborted Fetuses.
    Shen Y; Zhang W; Hua P; Qian F
    Altern Ther Health Med; 2024 Oct; 30(10):384-390. PubMed ID: 38401069
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Prenatal diagnosis and genetic analysis of two fetuses with Wolf-Hirschhorn syndrome].
    Li F; Wu A; Xie X; Ma M; Tang J; Tang S; Tan W; Yin W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Oct; 41(10):1201-1205. PubMed ID: 39344614
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Prenatal diagnosis of Jacobsen syndrome in a fetus carried by a pregnant woman with intellectual disability].
    Guo C; Wang J; Tang Y; Shi H; Liu J; Zhao L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug; 36(8):826-288. PubMed ID: 31400138
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genetic analysis of a fetus with mosaicism of structural aberration of Y chromosome].
    Xing H; Yang K
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Dec; 38(12):1250-1253. PubMed ID: 34839518
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Prenatal diagnosis of a fetus with 8q13.3 microdeletion through chromosomal microarray analysis].
    Rao H; Liu Y; Xiao J; Zou Y; Yuan H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):268-270. PubMed ID: 33751539
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical phenotype and genetic analysis of a fetus with recombinant chromosome 8 syndrome].
    Hao W; Zhang Y; Wang Y; Xie L; Yu X; Lyu J; Che Y; Xu J; Jia Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):1036-1040. PubMed ID: 37532508
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of a heritable partial monosomy 18p by molecular and cytogenetic analysis.
    Rigola MA; Plaja A; Mediano C; Miró R; Egozcue J; Fuster C
    Am J Med Genet; 2001 Nov; 104(1):37-41. PubMed ID: 11746025
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.