Pages that link to "Q33594628"
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The following pages link to Minimal expression of myotonic dystrophy: a clinical and molecular analysis (Q33594628):
Displaying 11 items.
- Instability versus predictability: the molecular diagnosis of myotonic dystrophy (Q33594617) (← links)
- Frequency of myotonic dystrophy gene carriers in cataract patients. (Q33683337) (← links)
- Investigation of muscle disease (Q33735060) (← links)
- Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure (Q34226936) (← links)
- Paternal transmission of the congenital form of myotonic dystrophy type 1: a new case and review of the literature (Q34504514) (← links)
- Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy (Q35194656) (← links)
- Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM). (Q35194760) (← links)
- The DMPK gene of severely affected myotonic dystrophy patients is hypermethylated proximal to the largely expanded CTG repeat (Q41968306) (← links)
- New genes for old diseases: the molecular basis of myotonic dystrophy and Huntington's disease. The Lumleian Lecture 1995. (Q45292726) (← links)
- Positive correlation of CTG expansion and pharyngoesophageal alterations in myotonic dystrophy patients (Q74145232) (← links)
- Fragile-X syndrome and myotonic dystrophy: parallels and paradoxes (Q74607477) (← links)