B. Udd
Neurological Department
Vasa Central Hospital
Finland
Name/email consistency: low
- Tibial muscular dystrophy--from clinical description to linkage on chromosome 2q31. Udd, B., Haravuori, H., Kalimo, H., Partanen, J., Pulkkinen, L., Paetau, A., Peltonen, L., Somer, H. Neuromuscul. Disord. (1998)
- Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?. Udd, B., Krahe, R., Wallgren-Pettersson, C., Falck, B., Kalimo, H. Neuromuscul. Disord. (1997)