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

محفوظ في:

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Rajan-Babu, Indhu-Shree, Lian, Mulias, Cheah, Felicia SH, Chen, Min, Tan, Arnold SC, Prasath, Ethiraj B, Loh, Seong Feei, Chong, Samuel S
مؤلفون آخرون:	DUKE-NUS MEDICAL SCHOOL
التنسيق:	Review
اللغة:	English
منشور في:	CAMBRIDGE UNIV PRESS 2022
الموضوعات:	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
الوصول للمادة أونلاين:	https://scholarbank.nus.edu.sg/handle/10635/226868
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
المؤسسة:	National University of Singapore
اللغة:	English

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