Literature DB >> 2870387

DNA deletion in boy with Becker muscular dystrophy.

S Hodgson, K Hart, A Walker, C Cole, L Johnson, M Bobrow, V Dubowitz, L Kunkel.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 2870387     DOI: 10.1016/s0140-6736(86)91023-8

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


× No keyword cloud information.
  4 in total

1.  DNA deletions in mild and severe Becker muscular dystrophy.

Authors:  K A Hart; S Hodgson; A Walker; C G Cole; L Johnson; V Dubowitz; M Bobrow
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

Review 2.  Diagnosis of genetic disease using recombinant DNA. Supplement.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

3.  Familial deletion in Becker type muscular dystrophy within the pXJ region.

Authors:  S Liechti-Gallati; S Braga; H Hirsiger; H Moser
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

4.  Linkage studies in Duchenne and Becker muscular dystrophies.

Authors:  A Walker; K Hart; C Cole; S Hodgson; L Johnson; V Dubowitz; M Bobrow
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.