Pages that link to "Q66694732"

The following pages link to Frequency of Duchenne muscular dystrophy carriers (Q66694732):

Displaying 14 items.

• A genetic study of Duchenne muscular dystrophy in West Midlands (Q33668368) (← links)
• Chimeric snRNA molecules carrying antisense sequences against the splice junctions of exon 51 of the dystrophin pre-mRNA induce exon skipping and restoration of a dystrophin synthesis in Delta 48-50 DMD cells (Q34035676) (← links)
• Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse (Q34582428) (← links)
• Effects of reproductive compensation and genetic drift on X-linked lethals (Q35202723) (← links)
• Dystrophin, its gene, and the dystrophinopathies (Q40373239) (← links)
• Duchenne muscular dystrophy. Frequency of sporadic cases (Q41576138) (← links)
• Human dystrophin gene transfer: production and expression of a functional recombinant DNA-based gene (Q42825904) (← links)
• A study of possible heterogeneity in Duchenne muscular dystrophy (Q43598511) (← links)
• Social selection and evolution of human diseases (Q45304899) (← links)
• Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases (Q45888931) (← links)
• Early diagnosis of Duchenne muscular dystrophy (Q66698603) (← links)
• Diagnosis, carrier detection, and genetic counseling in the muscular dystrophies (Q67382297) (← links)
• Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different ages (Q67895743) (← links)
• High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling (Q78048699) (← links)