Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.

Author:

Bakker E,Veenema H,Den Dunnen J T,van Broeckhoven C,Grootscholten P M,Bonten E J,van Ommen G J,Pearson P L

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference24 articles.

1. Duchenne muscular dystrophy;Emery, A.E.H.,1988

2. Prenatal diagnosis and carrier-detection of Duchenne muscular dystrophy with closely linked RFLPs;Bakker, E.; Hofker, M.H.; Goor, N.;Lancet,1985

3. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure;Bakker, E.; Bonten, E.J.; de Lange, L.F.;J Med Genet,1986

4. Prenatal diagnosis of Duchenne muscular dystrophy: a three year experience in a rapidly evolving field;Bakker, E.; Bonten, E.J.; Veenema, H.;J Inherited Metab Dis; Prenatal diagnosis and detection of carriers with DNA probes in Duchenne's muscular dystrophy,1987

5. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA;Darras, B.T.; Koenig, M.; Kunkel, L.M.; Francke, U.;Am J Med Genet,1988

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