FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome

FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome

10.1017/erm.2017.10

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書目詳細資料
Main Authors:	Rajan-Babu, Indhu-Shree, Lian, Mulias, Cheah, Felicia SH, Chen, Min, Tan, Arnold SC, Prasath, Ethiraj B, Loh, Seong Feei, Chong, Samuel S
其他作者:	DUKE-NUS MEDICAL SCHOOL
格式:	Review
語言:	English
出版:	CAMBRIDGE UNIV PRESS 2022
主題:	Science & Technology Life Sciences & Biomedicine Biochemistry & Molecular Biology Medicine, Research & Experimental Research & Experimental Medicine MULTIPLE DISPLACEMENT AMPLIFICATION FULL-MUTATION PRIMED PCR PRACTICE GUIDELINES MYOTONIC-DYSTROPHY EXPANDED ALLELES PREMUTATION DNA CARRIERS DISEASE
在線閱讀:	https://scholarbank.nus.edu.sg/handle/10635/226868
標簽:	添加標簽沒有標簽, 成為第一個標記此記錄!
機構:	National University of Singapore
語言:	English

實物特徵
總結:	10.1017/erm.2017.10