We conducted prenatal diagnosis by haplotype analysis, using newly developed microsatellite markers, in eight Fukuyama type congenital muscular dystrophy (FCMD) families. In addition to six new families, two previously reported families were reexamined by haplotype analysis including detection of an
✦ LIBER ✦
The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophy
✍ Scribed by Isam Naom; Mariella D’Alessandro; Caroline Sewry; Alessandra Ferlini; Haluk Topaloglu; Anne Helbling-Leclerc; Pascale Guicheney; Ketty Schwartz; Zuhal Akcoren; Victor Dubowitz; F. Muntoni
- Publisher
- Springer
- Year
- 1997
- Tongue
- English
- Weight
- 387 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0340-6717
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