14 results on '"Tome, F."'
Search Results
2. Autosomal recessive oculopharyngodistal myopathy in light of distal myopathy with rimmed vacuoles and oculopharyngeal muscular dystrophy
3. Oculopharyngeal muscular dystrophy in Italy
4. Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy
5. Oculopharyngeal muscular dystrophy in France
6. Oculopharyngeal muscular dystrophy in Japan
7. Genealogical study of oculopharyngeal muscular dystrophy in France
8. Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene
9. Chromosome 15-linked limb-girdle muscular dystrophy: clinical phenotypes in Reunion Island and French metropolitan communities
10. Abstracts from the Third International Symposium on Familial Amyloidotic Polyneuropathy and Other TTR Related Disorders Second International Workshop on Liver Transplantation in FAP held in Lisbon, 27-29 October 1995
11. Expression of dystrophin-associated glyocoproteins during human fetal muscle development: a preliminary immunocytochemical study
12. The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies
13. Ubiquitin and -amyloid-protein in inclusion body myositis (IBM), familial IBM-like disorder and oculopharyngeal muscular dystrophy: an immunocytochemical study
14. Merosin-negative congenital muscular dystrophy, cortical dysplasia and epilepsy: An association to investigate
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