Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHD.

Author:

Upadhyaya M,Maynard J,Rogers M T,Lunt P W,Jardine P,Ravine D,Harper P S

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. Diagnostic criteria for facioscapulohumeral muscular dystrophy;Padberg, G.W.; Lunt, P.W.; Koch, M.; Fardeau, M.;Neuronmuisc Disord,1991

2. Genetic counselling in facioscapulohumeral muscular dystrophy;Lunt, P.W.; Harper, P.S.;JMed Genet,1991

3. Location of facioscapulohumeral muscular dystrophy gene on chromosome 4;Wijmenga, C.; Frants, R.R.; Brouwer, O.F.; Moerer, P.; Weber, J.L.; Padberg, G.W.;Lancet,1990

4. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy;Wijmenga, C.; Hewitt, J.E.; Sandkujil, L.A.;Nat Genet,1992

5. Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements;Upadhyaya, M.; Jardine, P.; Maynard, J.;Hum Mol Genet,1993

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