Evaluation of an in-house protocol for prenatal molecular diagnosis of SMA in Chinese-Reference-Cited by-同舟云学术

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Evaluation of an in-house protocol for prenatal molecular diagnosis of SMA in Chinese

Published:2008-12 Issue:1-2 Volume:398 Page:78-81
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Zeng Jian,Lan Fenghua,Deng Xiaojun,Ke Longfeng,Tu Xiangdong,Huang Lianghu,Zheng Dezhu,Zhu Zhongyong

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference15 articles.

1. Spinal muscular atrophy genetic testing experience at an academic medical center;Ogino;J Mol Diagn,2002

2. Identification and characterization of a spinal muscular atrophy-determining gene;Lefebvre;Cell,1995

3. PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophy;Van der Steege;Lancet,1995

4. Allele-specific amplification for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy;Moutou;Prenat Diagn,2001

5. Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification;Schouten;Nucleic Acids Res,2002

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A simple and precise diagnostic method for spinal muscular atrophy using a quantitative SNP analysis system;ELECTROPHORESIS;2014-10-09

2. Multiplex ligation-dependent probe amplification (MLPA) and prenatal diagnosis;Prenatal Diagnosis;2012-03-30

3. Establishment of a Molecular Diagnostic System for Spinal Muscular Atrophy;The Journal of Molecular Diagnostics;2011-01

4. Universal fluorescent multiplex PCR and capillary electrophoresis for evaluation of gene conversion between SMN1 and SMN2 in spinal muscular atrophy;Analytical and Bioanalytical Chemistry;2010-06-19

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