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 *

161 related articles for article (PubMed ID: 37277873)

  • 1. Preimplantation genetic testing for Aicardi-Goutières syndrome induced by novel compound heterozygous mutations of TREX1: an unaffected live birth.
    Xu H; Pu J; Lin S; Hu R; Yao J; Li X
    Mol Cytogenet; 2023 Jun; 16(1):9. PubMed ID: 37277873
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical application of NGS-based SNP haplotyping for PGT-M of methylmalonic acidemia.
    He B; Wang L; Wu Q; Wang X; Ji X; Shi W; Shi J; Qiang R; Zhen S
    Syst Biol Reprod Med; 2022 Feb; 68(1):80-88. PubMed ID: 34913786
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Affected-embryo-based SNP haplotyping with NGS for the preimplantation genetic testing of Marfan syndrome.
    Deng Y; Ou Z; Li R; Chen Z; Liang P; Sun L
    Syst Biol Reprod Med; 2021 Aug; 67(4):298-306. PubMed ID: 34053377
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical application of NGS-based SNP haplotyping for the preimplantation genetic diagnosis of primary open angle glaucoma.
    Ji X; Zhang Z; Shi J; He B
    Syst Biol Reprod Med; 2019 Jun; 65(3):258-263. PubMed ID: 30977407
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comprehensive preimplantation genetic testing by massively parallel sequencing.
    Chen S; Yin X; Zhang S; Xia J; Liu P; Xie P; Yan H; Liang X; Zhang J; Chen Y; Fei H; Zhang L; Hu Y; Jiang H; Lin G; Chen F; Xu C
    Hum Reprod; 2021 Jan; 36(1):236-247. PubMed ID: 33306794
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Preimplantation Genetic Testing for Rare Inherited Disease of MMA-CblC: an Unaffected Live Birth.
    Peng C; Ren J; Li Y; Keqie Y; Zhou F; Zhang X; Zhu H; Hu T; Wang H; Chen X; Liu S
    Reprod Sci; 2021 Dec; 28(12):3571-3578. PubMed ID: 34076870
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel multifunctional haplotyping-based preimplantation genetic testing for different genetic conditions.
    Xie P; Hu X; Kong L; Mao Y; Cheng D; Kang K; Dai J; Zhao D; Zhang Y; Lu N; Wan Z; Du R; Xiong B; Zhang J; Tan Y; Lu G; Gong F; Lin G; Liang B; Du J; Hu L
    Hum Reprod; 2022 Oct; 37(11):2546-2559. PubMed ID: 36066440
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Preimplantation genetic testing for monogenic disorders (PGT-M) offers an alternative strategy to prevent children from being born with hereditary neurological diseases or metabolic diseases dominated by nervous system phenotypes: a retrospective study.
    Zou W; Li M; Wang X; Lu H; Hao Y; Chen D; Zhu S; Ji D; Zhang Z; Zhou P; Cao Y
    J Assist Reprod Genet; 2024 May; 41(5):1245-1259. PubMed ID: 38470552
    [TBL] [Abstract][Full Text] [Related]  

  • 9. GENType: all-in-one preimplantation genetic testing by pedigree haplotyping and copy number profiling suitable for third-party reproduction.
    De Witte L; Raman L; Baetens M; De Koker A; Callewaert N; Symoens S; Tilleman K; Vanden Meerschaut F; Dheedene A; Menten B
    Hum Reprod; 2022 Jun; 37(7):1678-1691. PubMed ID: 35552408
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Eleven healthy live births: a result of simultaneous preimplantation genetic testing of α- and β-double thalassemia and aneuploidy screening.
    Chen D; Shen X; Wu C; Xu Y; Ding C; Zhang G; Xu Y; Zhou C
    J Assist Reprod Genet; 2020 Mar; 37(3):549-557. PubMed ID: 32152910
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Proband-independent haplotyping based on NGS-based long-read sequencing for detecting pathogenic variant carrier status in preimplantation genetic testing for monogenic diseases.
    Zhang P; Zhao X; Li Q; Xu Y; Cheng Z; Yang L; Wang H; Tao Y; Huang G; Wu R; Zhou H; Zhao S
    Front Mol Biosci; 2024; 11():1329580. PubMed ID: 38516188
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Case report: Preimplantation genetic testing for X-linked alport syndrome caused by variation in the
    Liu N; Wen X; Ou Z; Fang X; Du J; Lin X
    Front Pediatr; 2023; 11():1177019. PubMed ID: 37635800
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing.
    Masset H; Zamani Esteki M; Dimitriadou E; Dreesen J; Debrock S; Derhaag J; Derks K; Destouni A; Drüsedau M; Meekels J; Melotte C; Peeraer K; Tšuiko O; van Uum C; Allemeersch J; Devogelaere B; François KO; Happe S; Lorson D; Richards RL; Theuns J; Brunner H; de Die-Smulders C; Voet T; Paulussen A; Coonen E; Vermeesch JR
    Hum Reprod; 2019 Aug; 34(8):1608-1619. PubMed ID: 31348829
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Complex preimplantation genetic tests for Robertsonian translocation, HLA, and X-linked hyper IgM syndrome caused by a novel mutation of CD40LG gene.
    Huang S; Niu Y; Li J; Gao M; Zhang Y; Yan J; Ma S; Gao X; Gao Y
    J Assist Reprod Genet; 2020 Aug; 37(8):2025-2031. PubMed ID: 32500460
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Minimizing mosaicism: assessing the impact of fertilization method on rate of mosaicism after next-generation sequencing (NGS) preimplantation genetic testing for aneuploidy (PGT-A).
    Palmerola KL; Vitez SF; Amrane S; Fischer CP; Forman EJ
    J Assist Reprod Genet; 2019 Jan; 36(1):153-157. PubMed ID: 30362056
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A whole-genome sequencing-based novel preimplantation genetic testing method for de novo mutations combined with chromosomal balanced translocations.
    Yuan P; Xia J; Ou S; Liu P; Du T; Zheng L; Yin X; Xie L; Zhang S; Yan H; Gao Y; Zhang Q; Jiang H; Chen F; Wang W
    J Assist Reprod Genet; 2020 Oct; 37(10):2525-2533. PubMed ID: 32783137
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Preimplantation genetic testing for monogenic/single gene disorders in a family with Molybdenum co-factor deficiency].
    Li Z; Zhou H; Shu J; Wang C; Huang P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Feb; 40(2):143-147. PubMed ID: 36709930
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M.
    Destouni A; Dimitriadou E; Masset H; Debrock S; Melotte C; Van Den Bogaert K; Zamani Esteki M; Ding J; Voet T; Denayer E; de Ravel T; Legius E; Meuleman C; Peeraer K; Vermeesch JR
    Hum Reprod; 2018 Dec; 33(12):2302-2311. PubMed ID: 30383227
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Next-generation sequence-based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism.
    Hu X; He WB; Zhang SP; Luo KL; Gong F; Dai J; Zhang Y; Wan ZX; Li W; Yuan SM; Tan YQ; Lu GX; Lin G; Du J
    Mol Genet Genomic Med; 2021 May; 9(5):e1662. PubMed ID: 33942572
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The true incidence of chromosomal mosaicism after preimplantation genetic testing is much lower than that indicated by trophectoderm biopsy.
    Wu L; Jin L; Chen W; Liu JM; Hu J; Yu Q; Ren XL; Huang B; He H
    Hum Reprod; 2021 May; 36(6):1691-1701. PubMed ID: 33860322
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.