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J-GLOBAL ID:202002252927624528   Reference number:20A2742430

一気にやって来た!産婦人科におけるゲノム医療時代 PGT-Mで診断できる疾患,できない疾患

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Volume: 27  Issue:Page: 293-297  Publication year: Dec. 01, 2020 
JST Material Number: L3856A  ISSN: 1340-220X  Document type: Article
Article type: 文献レビュー  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Gynecologic and obstetric diagnosis  ,  Diagnostics of congenital diseases, deformities. 
Reference (10):
  • 日本産科婦人科学会倫理委員会 着床前診断に関する審査小委員会(委員長: 榊原秀也). 倫理委員会 着床前診断に関する審査小委員会報告(1999~2015年度分の着床前診断の認可状況および実施成績). 日産婦会誌. 2017; 69: 1916-20.
  • Richards S, Aziz N, Bale S, et al ; ACMG Laboratory Quality Assurance Committee. Standards and guidelines for the interpretation of sequence variants : a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015 ; 17 : 405-24.
  • 日本産科婦人科学会. 「着床前診断」に関する見解. 日産婦会誌. 2018; 70: 1854-5
  • Kurahashi H, Kato T, Miyazaki J, et al. Preimplantation genetic diagnosis/screening by comprehensive molecular testing. Reprod Med Biol. 2015 ; 15 : 13-9.
  • Huang L, Ma F, Chapman A, et al. Single-Cell Whole-Genome Amplification and Sequencing : Methodology and Applications. Annu Rev Genomics Hum Genet. 2015 ; 16 : 79-102.
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