PCR Approach for Detection of Fragile X Syndrome and Huntington Disease Based on Modified DNA: Limits and Utility-Reference-Cited by-同舟云学术

PCR Approach for Detection of Fragile X Syndrome and Huntington Disease Based on Modified DNA: Limits and Utility

Published:2007-06 Issue:2 Volume:11 Page:153-159
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Rosales-Reynoso Mónica Alejandra¹,Vilatela Elisa Alonso²,Ojeda Rosario Macias²,Arce-Rivas Aura³,Sandoval Lucila¹,Troyo-Sanromán Rogelio⁴,Barros-Núñez Patricio¹

Affiliation:

1. División de Genética, CIBO, Instituto Mexicano del Seguro Social. Guadalajara, México.

2. Departamento de Genética, Instituto Nacional de Neurología y Neurocirugía “Manuel Velasco Suárez,” México, DF.

3. Universidad Autónoma de Mexicali, BC. México.

4. Departamento de Fisiología, CUCS, Universidad de G. Guadalajara, México.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/gte.2006.0508

Reference44 articles.

1. Analysis of the (CAG)n repeat causing Huntington's disease in a Mexican population

2. Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome

3. Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test

4. Chemiluminescent detection of blotted PCR products (CB-PCR) of two CAG dynamic mutations (Huntington's disease and spinocerebellar ataxia type 1).

5. Robust amplification and ethidium-visible detection of the fragile X syndrome CGG repeat usingPfu polymerase

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