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.
155 related articles for article (PubMed ID: 37117255)
1. Gene sequencing and result analysis of balanced translocation carriers by third-generation gene sequencing technology. Zeng X; Lin D; Liang D; Huang J; Yi J; Lin D; Zhang Z Sci Rep; 2023 Apr; 13(1):7004. PubMed ID: 37117255 [TBL] [Abstract][Full Text] [Related]
2. Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore Platform. Hu L; Liang F; Cheng D; Zhang Z; Yu G; Zha J; Wang Y; Xia Q; Yuan D; Tan Y; Wang D; Liang Y; Lin G Front Genet; 2019; 10():1313. PubMed ID: 32010185 [TBL] [Abstract][Full Text] [Related]
3. Analysis of Preimplantation and Clinical Outcomes of Two Cases by Oxford Nanopore Sequencing. Ou J; Wang J; Sun J; Ni M; Meng Q; Ding J; Fan H; Feng S; Huang Y; Li H; Fei J Reprod Sci; 2024 Jul; 31(7):2123-2134. PubMed ID: 38347380 [TBL] [Abstract][Full Text] [Related]
4. Identifying Balanced Chromosomal Translocations in Human Embryos by Oxford Nanopore Sequencing and Breakpoints Region Analysis. Pei Z; Deng K; Lei C; Du D; Yu G; Sun X; Xu C; Zhang S Front Genet; 2021; 12():810900. PubMed ID: 35116057 [No Abstract] [Full Text] [Related]
5. Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations. Liang D; Wang Y; Ji X; Hu H; Zhang J; Meng L; Lin Y; Ma D; Jiang T; Jiang H; Asan ; Song L; Guo J; Hu P; Xu Z Clin Genet; 2017 Apr; 91(4):605-610. PubMed ID: 27491356 [TBL] [Abstract][Full Text] [Related]
6. Distinguishing between carrier and noncarrier embryos with the use of long-read sequencing in preimplantation genetic testing for reciprocal translocations. Chow JFC; Cheng HHY; Lau EYL; Yeung WSB; Ng EHY Genomics; 2020 Jan; 112(1):494-500. PubMed ID: 30946890 [TBL] [Abstract][Full Text] [Related]
7. Translocation breakpoints of chromosome 4 in male carriers: clinical features and implications for genetic counseling. Zhang HG; Wang RX; Pan Y; Zhu JH; Xue LT; Yang X; Liu RZ Genet Mol Res; 2016 Dec; 15(4):. PubMed ID: 27966754 [TBL] [Abstract][Full Text] [Related]
8. Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing. Aristidou C; Koufaris C; Theodosiou A; Bak M; Mehrjouy MM; Behjati F; Tanteles G; Christophidou-Anastasiadou V; Tommerup N; Sismani C PLoS One; 2017; 12(1):e0169935. PubMed ID: 28072833 [TBL] [Abstract][Full Text] [Related]
9. Breakpoint mapping of a novel de novo translocation t(X;20)(q11.1;p13) by positional cloning and long read sequencing. Dutta UR; Rao SN; Pidugu VK; V S V; Bhattacherjee A; Bhowmik AD; Ramaswamy SK; Singh KG; Dalal A Genomics; 2019 Sep; 111(5):1108-1114. PubMed ID: 30006036 [TBL] [Abstract][Full Text] [Related]
10. Using short read sequencing to characterise balanced reciprocal translocations in pigs. Bouwman AC; Derks MFL; Broekhuijse MLWJ; Harlizius B; Veerkamp RF BMC Genomics; 2020 Aug; 21(1):576. PubMed ID: 32831014 [TBL] [Abstract][Full Text] [Related]
11. Translocation breakpoints of chromosome 3 in male carriers: a report of twelve cases and a review of the literature. Zhang H; Wang R; Li L; Zhu H; Zhang H; Liu R Turk J Med Sci; 2018 Feb; 48(1):150-156. PubMed ID: 29479975 [TBL] [Abstract][Full Text] [Related]
12. Precise detection of chromosomal translocation or inversion breakpoints by whole-genome sequencing. Suzuki T; Tsurusaki Y; Nakashima M; Miyake N; Saitsu H; Takeda S; Matsumoto N J Hum Genet; 2014 Dec; 59(12):649-54. PubMed ID: 25296578 [TBL] [Abstract][Full Text] [Related]
13. Historical and Clinical Perspectives on Chromosomal Translocations. Wilch ES; Morton CC Adv Exp Med Biol; 2018; 1044():1-14. PubMed ID: 29956287 [TBL] [Abstract][Full Text] [Related]
14. 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; 38(3):709-718. PubMed ID: 33409753 [TBL] [Abstract][Full Text] [Related]
15. Chromosomal analysis for embryos from balanced chromosomal rearrangement carriers using next generation sequencing. Ma X; Xu X; Mao B; Liu H; Li H; Liu K; Song D; Xue S; Wang N Mol Reprod Dev; 2021 May; 88(5):362-370. PubMed ID: 33783068 [TBL] [Abstract][Full Text] [Related]
16. Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to Murcia Pienkowski V; Kucharczyk M; Młynek M; Szczałuba K; Rydzanicz M; Poszewiecka B; Skórka A; Sykulski M; Biernacka A; Koppolu AA; Posmyk R; Walczak A; Kosińska J; Krajewski P; Castaneda J; Obersztyn E; Jurkiewicz E; Śmigiel R; Gambin A; Chrzanowska K; Krajewska-Walasek M; Płoski R J Med Genet; 2019 Feb; 56(2):104-112. PubMed ID: 30352868 [TBL] [Abstract][Full Text] [Related]
17. Clinical feature of infertile men carrying balanced translocations involving chromosome 10: Case series and a review of the literature. Zhang H; Wang R; Li L; Jiang Y; Zhang H; Liu R Medicine (Baltimore); 2018 Apr; 97(15):e0452. PubMed ID: 29642220 [TBL] [Abstract][Full Text] [Related]
18. Reciprocal Translocation Carrier Diagnosis in Preimplantation Human Embryos. Hu L; Cheng D; Gong F; Lu C; Tan Y; Luo K; Wu X; He W; Xie P; Feng T; Yang K; Lu G; Lin G EBioMedicine; 2016 Dec; 14():139-147. PubMed ID: 27840008 [TBL] [Abstract][Full Text] [Related]
19. Nanopore sequencing for detecting reciprocal translocation carrier status in preimplantation genetic testing. Xia Q; Li S; Ding T; Liu Z; Liu J; Li Y; Zhu H; Yao Z BMC Genomics; 2023 Jan; 24(1):1. PubMed ID: 36593441 [TBL] [Abstract][Full Text] [Related]
20. Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders. Schluth-Bolard C; Diguet F; Chatron N; Rollat-Farnier PA; Bardel C; Afenjar A; Amblard F; Amiel J; Blesson S; Callier P; Capri Y; Collignon P; Cordier MP; Coubes C; Demeer B; Chaussenot A; Demurger F; Devillard F; Doco-Fenzy M; Dupont C; Dupont JM; Dupuis-Girod S; Faivre L; Gilbert-Dussardier B; Guerrot AM; Houlier M; Isidor B; Jaillard S; Joly-Hélas G; Kremer V; Lacombe D; Le Caignec C; Lebbar A; Lebrun M; Lesca G; Lespinasse J; Levy J; Malan V; Mathieu-Dramard M; Masson J; Masurel-Paulet A; Mignot C; Missirian C; Morice-Picard F; Moutton S; Nadeau G; Pebrel-Richard C; Odent S; Paquis-Flucklinger V; Pasquier L; Philip N; Plutino M; Pons L; Portnoï MF; Prieur F; Puechberty J; Putoux A; Rio M; Rooryck-Thambo C; Rossi M; Sarret C; Satre V; Siffroi JP; Till M; Touraine R; Toutain A; Toutain J; Valence S; Verloes A; Whalen S; Edery P; Tabet AC; Sanlaville D J Med Genet; 2019 Aug; 56(8):526-535. PubMed ID: 30923172 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]