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 *

150 related articles for article (PubMed ID: 36585011)

  • 1. [Prenatal diagnosis for a fetus with 5p deletion syndrome].
    Wang J; Zhang W; Yang H; Ma X; Li J; Chen X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jan; 40(1):101-104. PubMed ID: 36585011
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. [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]  

  • 4. [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]  

  • 5. Prenatal diagnosis of Cri-du-Chat syndrome with concomitant distal trisomy 10q syndrome in one fetus with ultrasound anomalies.
    He JP; Qian Y; Liu WJ; Tang J; Qin MH; Luo SJ; Hou JH; Lv MX
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):318-323. PubMed ID: 33678334
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].
    Hu JC; Tan K; Cheng DH; Li LY; Lu GX; Tan YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):87-90. PubMed ID: 23450488
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies.
    Zhang J; Zhang B; Liu T; Xie H; Zhai J
    Mol Cytogenet; 2020; 13():26. PubMed ID: 32625247
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Analysis of copy number variations in an infant with Cri du Chat syndrome by array-based comparative genomic hybridization].
    Luo FW; Luo CQ; Xie JS; Gen Q; Liu H; Li F; Chen WB; Wang L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):443-6. PubMed ID: 23926013
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. Prenatal diagnosis of 5p-.
    David K; Kaffe S; Strauss L; Hsu LY; Serotkin A; Hirschhorn K
    Clin Genet; 1978 Feb; 13(2):224-8. PubMed ID: 627112
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Prenatal genetic analysis of a fetus with Miller-Dieker syndrome].
    Wang F; Qi N; Wang T; Gao Y; Wu D; Zhang M; Yang K; Peng H; Lei X; Liao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Apr; 40(4):505-511. PubMed ID: 36972951
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetic analysis of a recurrent abnormal pregnancy case caused by a cryptic reciprocal autosomal translocation].
    He T; Tao D; Liu Y; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Dec; 38(12):1241-1244. PubMed ID: 34839516
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Partial translocation of NOR and its activity in a balanced carrier and in her cri-du-chat fetus.
    Dev VG; Byrne J; Bunch G
    Hum Genet; 1979 Oct; 51(3):277-80. PubMed ID: 511156
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Cytogenetic analysis of an amniotic sample with X chromosome abnormality signaled by non-invasive prenatal testing].
    Zhang W; Zhang W; Pan F; Wang D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Jun; 38(6):573-576. PubMed ID: 34096029
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Application of genomic copy number variation detection technology in prenatal diagnosis of 7617 pregnant women with serological screening abnormalities during the second trimester of pregnancy].
    Huang J; Wu D; Gao Y; Li Q; Zhang C; He J; Li X; Wang H; Guo Q; Lou G; Wang Y; Liu H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 May; 39(5):468-473. PubMed ID: 35598259
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genetic analysis of a fetus with mosaicism Y chromosome aberration].
    Meng F; Ju D; Wang X; Shi Y; Yang M; Li X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Nov; 40(11):1414-1419. PubMed ID: 37906152
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Analysis of a fetus with unbalanced translocation derived from a balanced t(6;14) maternal translocation].
    Zhang M; Xiao H; Wu D; Wang H; Gao Y; Zhang Q; Wang F; Wang T; Liao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Feb; 40(2):230-233. PubMed ID: 36709947
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. [Application of array comparative genomic hybridization in prenatal diagnosis of a case with 5q35 deletion syndrome].
    Feng Z; Hu H; Mao C; Wang D; Liu L; Liu S; Jing Z; Liu H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):240-243. PubMed ID: 28397228
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.