Benign Duchenne muscular dystrophy in a patient with growth hormone deficiency: A five years follow‐up
- 1 July 1986
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 24 (3) , 567-572
- https://doi.org/10.1002/ajmg.1320240323
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- X;autosome translocations in females with Duchenne or Becker muscular dystrophyNature, 1986
- Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9)Human Genetics, 1985
- Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequencesHuman Genetics, 1984
- Corresponding editor's column: Suggestion for a possible mitigating treatment of duchenne muscular dystrophyAmerican Journal of Medical Genetics, 1981
- Begnign duchenne muscular dystrophy in a patient with growth hormone deficiencyAmerican Journal of Medical Genetics, 1981
- Clinical studies in benign (Becker type) X‐linked muscular dystrophyClinical Genetics, 1976