Comparison Between the Polymerase Chain Reaction-Based Screening and the Southern Blot Methods for Identification of Fragile X Syndrome-Reference-Cited by-同舟云学术

Comparison Between the Polymerase Chain Reaction-Based Screening and the Southern Blot Methods for Identification of Fragile X Syndrome

Published:2012-11 Issue:11 Volume:16 Page:1303-1308
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Curtis-Cioffi Karen M. Carvalho¹,Rodrigueiro Debora Aparecida²,Rodrigues Valter Curi³,Cicarelli Regina M. Barretto⁴,Scarel-Caminaga Raquel Mantuaneli¹

Affiliation:

1. Department of Morphology, UNESP, Univ Estadual Paulista, School of Dentistry in Araraquara, Araraquara, Brazil.

2. Department of Morphology and Pathology, PUC-SP, Pontifical Catholic University, School of Medical and Health Sciences, Sorocaba, Brazil.

3. Department of Medicine, UNIARA, University Center Araraquara, Araraquara, Brazil.

4. Department of Biological Sciences, UNESP, Univ Estadual Paulista, School of Pharmaceutical Sciences, Araraquara, Brazil.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2012.0158

Reference22 articles.

1. An Information-Rich CGG Repeat Primed PCR That Detects the Full Range of Fragile X Expanded Alleles and Minimizes the Need for Southern Blot Analysis

2. Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA

3. FMR1 and the fragile X syndrome: Human genome epidemiology review

4. A Homogeneous Assay for Analysis of FMR1 Promoter Methylation in Patients with Fragile X Syndrome

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