Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene-Reference-Cited by-同舟云学术

Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene

Published:1997-10 Issue: Volume:7 Page:S70-S74
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Brais Bernard,Bouchard Jean-Pierre,Gosselin France,Xie Ya-Gang,Fardeau Michel,Tomé Fernando M.S.,Rouleau Guy A.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference22 articles.

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2. Ptosis héréditaires familial et tardif des paupières supérieures. Pharyngoplégie également héréditaire et familiale concomittante;Amyot;Union Med Can,1948

3. Hereditary, familial and acquired ptosis of late onset;Amyot;Can Med Assoc J,1948

4. The clinical significance of ptosis with special reference to ptosis of late onset;Saucier;J Nerv Ment Dis,1954

5. Oculopharyngeal muscular dystrophy: familial disease of late life characterized by dysphagia and progressive ptosis of the eyelids;Victor;N Engl J Med,1962

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