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PUBMED FOR HANDHELDS

Journal Abstract Search


135 related items for PubMed ID: 37957533

  • 1. High-resolution PGT-A results in incidental identification of patients with small pathogenic copy number variants.
    Leahy D, Marin D, Xu J, Eccles J, Treff NR.
    J Assist Reprod Genet; 2024 Jan; 41(1):121-126. PubMed ID: 37957533
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  • 2. 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
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  • 3. 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 31; 37(11):2546-2559. PubMed ID: 36066440
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  • 4. Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do?
    Rotshenker-Olshinka K, Srebnik Moshe N, Weiss O, Shaviv S, Freireich O, Segel R, Zeligson S, Eldar-Geva T, Altarescu G.
    J Assist Reprod Genet; 2021 Mar 31; 38(3):719-725. PubMed ID: 33443723
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  • 5. Confirmation and pathogenicity of small copy number variations incidentally detected via a targeted next-generation sequencing-based preimplantation genetic testing for aneuploidy platform.
    Iturriaga A, Mounts E, Picchetta L, Vega C, Mulas F, Ottolini CS, Whitehead C, Tao X, Zhan Y, Loia N, Jobanputra V, Capalbo A, Jalas C.
    Fertil Steril; 2024 Nov 31; 122(5):789-798. PubMed ID: 38996904
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  • 7. The use of copy number loads to designate mosaicism in blastocyst stage PGT-A cycles: fewer is better.
    Girardi L, Figliuzzi M, Poli M, Serdarogullari M, Patassini C, Caroselli S, Pergher I, Cogo F, Coban O, Boynukalin FK, Bahceci M, Navarro R, Rubio C, Findikli N, Simón C, Capalbo A.
    Hum Reprod; 2023 May 02; 38(5):982-991. PubMed ID: 36928183
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  • 8. Preliminary analysis of numerical chromosome abnormalities in reciprocal and Robertsonian translocation preimplantation genetic diagnosis cases with 24-chromosomal analysis with an aCGH/SNP microarray.
    Xie Y, Xu Y, Wang J, Miao B, Zeng Y, Ding C, Gao J, Zhou C.
    J Assist Reprod Genet; 2018 Jan 02; 35(1):177-186. PubMed ID: 28921398
    [Abstract] [Full Text] [Related]

  • 9. Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing.
    Tsuiko O, El Ayeb Y, Jatsenko T, Allemeersch J, Melotte C, Ding J, Debrock S, Peeraer K, Vanhie A, De Leener A, Pirard C, Kluyskens C, Denayer E, Legius E, Vermeesch JR, Brems H, Dimitriadou E.
    Hum Reprod; 2023 Mar 01; 38(3):511-519. PubMed ID: 36625546
    [Abstract] [Full Text] [Related]

  • 10. Preimplantation genetic testing for structural rearrangement based on low-coverage next-generation sequencing accurately discriminates between normal and carrier embryos for patients with translocations.
    Zhai F, Wang Y, Li H, Wang Y, Zhu X, Kuo Y, Guan S, Li J, Song S, He Q, An J, Zhi X, Lian Y, Huang J, Li R, Qiao J, Yan L, Yan Z.
    Reprod Biomed Online; 2022 Sep 01; 45(3):473-480. PubMed ID: 35780041
    [Abstract] [Full Text] [Related]

  • 11. The application of PGT-A for carriers of balanced structural chromosomal rearrangements.
    Fodina V, Dudorova A, Alksere B, Dzalbs A, Vedmedovska N, Andersone S, Una C, Juris E, Dace B.
    Gynecol Endocrinol; 2019 Sep 01; 35(sup1):18-23. PubMed ID: 31532310
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  • 13. Evaluation of chromosomal abnormalities from preimplantation genetic testing to the reproductive outcomes: a comparison between three different structural rearrangements based on next-generation sequencing.
    Yuan P, Zheng L, Ou S, Zhao H, Li R, Luo H, Tan X, Zhang Q, Wang W.
    J Assist Reprod Genet; 2021 Mar 01; 38(3):709-718. PubMed ID: 33409753
    [Abstract] [Full Text] [Related]

  • 14. Clinical application of next-generation sequencing in preimplantation genetic diagnosis cycles for Robertsonian and reciprocal translocations.
    Zhang W, Liu Y, Wang L, Wang H, Ma M, Xu M, Xu X, Gao Z, Duan J, Cram DS, Yao Y.
    J Assist Reprod Genet; 2016 Jul 01; 33(7):899-906. PubMed ID: 27167073
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  • 15. Single-cell multi-omics sequencing reveals chromosome copy number inconsistency between trophectoderm and inner cell mass in human reconstituted embryos after spindle transfer.
    Zhong W, Shen K, Xue X, Wang W, Wang W, Zuo H, Guo Y, Yao S, Sun M, Song C, Wang Q, Ruan Z, Yao X, Shang W.
    Hum Reprod; 2023 Nov 02; 38(11):2137-2153. PubMed ID: 37766497
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