Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination-Reference-Cited by-同舟云学术

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Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination

Published:2005 Issue:11 Volume:25 Page:1011-1014
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Percesepe Antonio,Ferrari Maurizio,Coviello Domenico,Zanussi Monica,Castagni Marina,Neri Isabella,Travi Maurizio,Forabosco Antonino,Tedeschi Silvana

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference15 articles.

1. Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene.

2. Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene

3. PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

4. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

5. Diagnosis of Duchenne and Becker Muscular Dystrophies by Polymerase Chain Reaction

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1. Duchenne Muscular Dystrophy Gene therapy;Current Gene Therapy;2022-11-18

2. Mejoras en el diagnóstico de distrofinopatías: ¿qué hemos aprendido después de 20 años?;Revista de Neurología;2011

3. Characteristics of Dystrophin Gene Mutations Among Chinese Patients as Revealed by Multiplex Ligation–Dependent Probe Amplification;Genetic Testing and Molecular Biomarkers;2009-02

4. Characteristics of Dystrophin Gene Mutations Among Chinese Patients as Revealed by Multiplex Ligation–Dependent Probe Amplification;Genetic Testing;2009-01-08

5. Current World Literature;Current Opinion in Obstetrics & Gynecology;2007-04

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