Literature DB >> 2563028

DNA probes in differential diagnosis of Becker muscular dystrophy and spinal muscular atrophy.

P W Lunt, W J Cumming, H Kingston, A P Read, R C Mountford, M Mahon, R Harris.   

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Year:  1989        PMID： 2563028     DOI： 10.1016/s0140-6736(89)91704-2

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

1.  Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias.

Authors:  P W Lunt; D A Compston; P S Harper
Journal:  J Med Genet       Date:  1989-12       Impact factor: 6.318

2.  Genetic counselling in facioscapulohumeral muscular dystrophy.

Authors:  P W Lunt; P S Harper
Journal:  J Med Genet       Date:  1991-10       Impact factor: 6.318

3.  Rapid detection of deletions in the Duchenne muscular dystrophy gene by PCR amplification of deletion-prone exon sequences.

Authors:  M Hentemann; J Reiss; M Wagner; D N Cooper
Journal:  Hum Genet       Date:  1990-02       Impact factor: 4.132
  3 in total

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