Carrier detection and prenatal molecular diagnosis in a Duchenne muscular dystrophy family without any affected relative available-Reference-Cited by-同舟云学术

Carrier detection and prenatal molecular diagnosis in a Duchenne muscular dystrophy family without any affected relative available

Published:2001-07 Issue:3 Volume:44 Page:149-153
ISSN:0003-3995
Container-title:Annales de Génétique
language:en
Short-container-title:Annales de Génétique

Author:

Alcántara M.A,García-Cavazos R,Hernández-U E,González-del Angel A,Carnevale A,Orozco L

Publisher

Elsevier BV

Subject

Genetics

Reference21 articles.

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2. High frequency of de novo deletions in mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling;Alcántara;Clin. Genet.,1999

3. Evaluación de la actividad de la creatinofosfocinasa (CPK) para la detección de portadoras de distrofia muscular tipo Duchenne en familias de la ciudad de Monterrey, México;Álvarez;Rev. Invest. Clin.,1990

4. Are there ethnic differences in deletions in the dystrophin gene?;Banerjee;Am. J. Med. Genet.,1997

5. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction;Beggs;Hum. Genet.,1990

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