Literature DB >> 2890056

Inherited deletion at Duchenne dystrophy locus in normal male.

J Koh, R J Bartlett, M A Pericak-Vance, M C Speer, L H Yamaoka, K Phillips, W Y Hung, P N Ray, R G Worton, J R Gilbert.   

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Year:  1987        PMID： 2890056     DOI： 10.1016/s0140-6736(87)91590-x

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


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  6 in total

1.  A normal male with an inherited deletion of one exon within the DMD gene.

Authors:  M Nordenskjöld; L Nicholson; L Edström; M Anvret; M Eiserman; C Slater; L Stolpe
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

2.  Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.

Authors:  B T Darras; P Blattner; J F Harper; A J Spiro; S Alter; U Francke
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

3.  Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree.

Authors:  G K Suthers; J I Manson; L M Stern; E A Haan; J C Mulley
Journal:  J Med Genet       Date:  1989-04       Impact factor: 6.318

4.  Deletion screening in patients with Duchenne muscular dystrophy.

Authors:  K Wulff; F H Herrmann; M C Wapenaar; M Wehnert
Journal:  J Neurol       Date:  1989-12       Impact factor: 4.849

Review 5.  On the nature of the Duchenne muscular dystrophy locus: a portion of a complex of related gene clusters of recent pseudoautosomal origin?

Authors:  J P Infante; V A Huszagh
Journal:  Mol Cell Biochem       Date:  1988-06       Impact factor: 3.396

6.  Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56a.

Authors:  F H Herrmann; K Wulff; M Schütz; M Wehnert
Journal:  Eur J Pediatr       Date:  1990-01       Impact factor: 3.183
  6 in total

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