Pages that link to "Q33594351"
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The following pages link to Investigation of a female manifesting Becker muscular dystrophy (Q33594351):
Displaying 7 items.
- Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis (Q33595768) (← links)
- X inactivation patterns in female monozygotic twins and their families (Q33675242) (← links)
- X-chromosome methylation ratios as indicators of chromosomal activity: evidence of intraindividual divergencies among tissues of different embryonal origin (Q71482721) (← links)
- X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes (Q71958937) (← links)
- Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter (Q72387817) (← links)
- Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study (Q77924716) (← links)
- Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy (Q78005705) (← links)