Xp21 DNA PROBE IN DIAGNOSIS OF MUSCULAR DYSTROPHY AND SPINAL MUSCULAR ATROPHY
- 25 February 1989
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 333 (8635) , 443
- https://doi.org/10.1016/s0140-6736(89)90044-5
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg‐Welander syndromeAmerican Journal of Medical Genetics, 1988
- Preferential deletion of exons in Duchenne and Becker muscular dystrophiesNature, 1987
- Becker's X-linked muscular dystrophy histological, enzyme-histochemical, and ultrastructural studies of two cases, originally reported by BeckerActa Neuropathologica, 1979