DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

E Bakker; E J Bonten; L F De Lange; H Veenema; D Majoor-Krakauer; M H Hofker; G J Van Ommen; P L Pearson

doi:10.1136/jmg.23.6.573

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Research Article

DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

Authors

E Bakker PubMed articles Google scholar articles
E J Bonten PubMed articles Google scholar articles
L F De Lange PubMed articles Google scholar articles
H Veenema PubMed articles Google scholar articles
D Majoor-Krakauer PubMed articles Google scholar articles
M H Hofker PubMed articles Google scholar articles
G J Van Ommen PubMed articles Google scholar articles
P L Pearson PubMed articles Google scholar articles

Citation

Bakker E, Bonten EJ, De Lange LF, et al

DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

Journal of Medical Genetics 1986;23:573-580.

Publication history

First published December 1, 1986.

Online issue publication

April 27, 2016

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