يعرض 1 - 10 نتائج من 303 نتيجة بحث عن '"PGT‐M"', وقت الاستعلام: 1.02s تنقيح النتائج
  1. 1
    دورية أكاديمية
    First case report of a successful delivery of a healthy boy by preimplantation genetic testing for Beckwith-Wiedemann syndrome

    المؤلفون: Banti, MariaAff1, IDs10815024031867_cor1, Kafetzis, Dimitrios

    المصدر: Journal of Assisted Reproduction and Genetics. :1-5

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  2. 2
    دورية أكاديمية
    A heatmap for expected cumulative live birth rate in preimplantation genetic testing for monogenic disorders and chromosomal structural rearrangements

    المؤلفون: Van Der Kelen, AnneloreAff1, IDs10815024031416_cor1, Keymolen, Kathelijn, Cools, Wilfried, De Vos, Anick, Pölsler, Laura, De Vos, Michel, Blockeel, Christophe, Fernandez-Gallardo, Elia, De Rycke, Martine, Berckmoes, Veerle, Verdyck, Pieter, Hes, Frederik Jan, Verpoest, WillemAff3, Aff4

    المصدر: Journal of Assisted Reproduction and Genetics. :1-9

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  3. 3
    دورية أكاديمية
    PGT-M for spinocerebellar ataxia type 1: development of a STR panel and a report of two clinical cases

    المؤلفون: Soloveva, Elena V.Aff1, IDs1081502403105w_cor1, Skleimova, Maria M., Minaycheva, Larisa I., Garaeva, Anna F., Zhigalina, Daria I., Churkin, Egor O., Okkel, Yulia V., Timofeeva, Oksana S.Aff2, Aff3, Petrov, Ilya A.Aff2, Aff3, Seitova, Gulnara N., Lebedev, Igor N., Stepanov, Vadim A.

    المصدر: Journal of Assisted Reproduction and Genetics. 41(5):1273-1283

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  4. 4
    دورية أكاديمية
    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

    المؤلفون: Zou, WeiweiAff1, Aff2, Aff3, IDs10815024030571_cor1, Li, MinAff1, Aff2, Aff3, Wang, XiaoleiAff1, Aff2, Aff3, Lu, HedongAff1, Aff2, Aff3, Hao, YanAff1, Aff3, Aff4, Chen, DaweiAff1, Aff3, Aff4, Zhu, ShashaAff1, Aff3, Aff4, Ji, DongmeiAff1, Aff4, Aff5, Zhang, ZhiguoAff1, Aff4, Aff5, Zhou, PingAff1, Aff2, Aff3, IDs10815024030571_cor10, Cao, YunxiaAff1, Aff2, Aff3, IDs10815024030571_cor11

    المصدر: Journal of Assisted Reproduction and Genetics. 41(5):1245-1259

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  5. 5
    دورية أكاديمية
    Preimplantation genetic testing in the current era, a review

    المؤلفون: Tian, YafeiAff1, Aff2, Li, Mingan, Yang, JingminAff1, Aff4, Chen, Hongyan, Lu, DaruAff2, Aff4, IDs0040402407370z_cor5

    المصدر: Archives of Gynecology and Obstetrics. 309(5):1787-1799

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  6. 6
    دورية أكاديمية
    Development of pre-implantation genetic testing protocol for monogenic disorders (PGT-M) of Hb H disease

    المؤلفون: Pannarai Somboonchai, Pimlak Charoenkwan, Sirivipa Piyamongkol, Worashorn Lattiwongsakorn, Tawiwan Pantasri, Wirawit Piyamongkol

    المصدر: BMC Genomics, Vol 25, Iss 1, Pp 1-10 (2024)

    مصطلحات موضوعية: Alpha-thalassemia, Hb H disease, Multiplex fluorescent PCR, Preimplantation genetics testing for monogenic disorders (PGT-M), Biotechnology, TP248.13-248.65, Genetics, QH426-470

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/1471-2164

    URL الوصول: https://doaj.org/article/7c62aea24d224adba5f2a8c596231028

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  7. 7
    دورية أكاديمية
    A healthy live birth after mosaic blastocyst transfer in preimplantation genetic testing for GATA1-related cytopenia combined with HLA matching

    المؤلفون: Huiling Xu, Jiajie Pu, Zhengzhong Wu, Yulong Huang, Chanlin Han, Xuemei Li

    المصدر: BMC Medical Genomics, Vol 17, Iss 1, Pp 1-8 (2024)

    مصطلحات موضوعية: PGT-M, HLA typing, GATA1, Mosaic blastocyst transfer, Internal medicine, RC31-1245, Genetics, QH426-470

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/1755-8794

    URL الوصول: https://doaj.org/article/72550d1c43054ca3adebc52c23fc14b8

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  8. 8
    دورية أكاديمية
    Case report: A healthy baby achieved after preimplantation genetic testing from an infertile woman with hereditary leiomyomatosis and renal cell cancer syndrome

    المؤلفون: Qianhui Hu, Qing Zhang, Mengxi Guo, Haixia Ding, Ji Xi, Meiling Zhang, Min Wang, Lin Zhang, Shuyuan Li, Dandan Wu, Wen Li

    المصدر: Frontiers in Medicine, Vol 11 (2024)

    مصطلحات موضوعية: case report, hereditary leiomyomatosis and renal cell cancer, PGT-M, embryo transplantation, uterine leiomyomas, Medicine (General), R5-920

    وصف الملف: electronic resource

    Relation: https://www.frontiersin.org/articles/10.3389/fmed.2024.1400694/full; https://doaj.org/toc/2296-858X

    URL الوصول: https://doaj.org/article/287fdead86c04e3da4c07eae07f7e2b4

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  9. 9
    دورية أكاديمية
    Robust preimplantation genetic testing of the common F8 Inv22 pathogenic variant of severe hemophilia A using a highly polymorphic multi-marker panel encompassing the paracentric inversion

    المؤلفون: Nguyen, Minh Tam, Nguyen, Thanh Tung, Nguyen, Duy Bac, Nguyen, Thi Mai, Nguyen, Kim Ngan, Ngo, Van Nhat Minh, Nguyen, Van Dieu, Tran, Ngoc Anh, Lian, Mulias, Tan, Arnold S. C., Chong, Samuel S.Aff3, Aff4, Aff5, Aff6, IDs1295902300552w_cor11, Dang, Tien TruongAff1, IDs1295902300552w_cor12

    المصدر: Thrombosis Journal. 21(1)

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  10. 10
    دورية أكاديمية
    A long-read sequencing and SNP haplotype-based novel preimplantation genetic testing method for female ADPKD patient with de novo PKD1 mutation

    المؤلفون: Peng, CuitingAff1, Aff2, Chen, HanAff1, Aff2, Ren, JunAff1, Aff2, Zhou, FanAff1, Aff2, Li, YutongAff1, Aff2, Keqie, YuezhiAff1, Aff2, Ding, Taoli, Ruan, Jiangxing, Wang, HeAff1, Aff2, Chen, XinlianAff1, Aff2, IDs1286402309593x_cor10, Liu, ShanlingAff1, Aff2, IDs1286402309593x_cor11

    المصدر: BMC Genomics. 24(1)

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