Female twin with hunter disease due to nonrandom inactivation of the X-chromosome: A consequence of twinning
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.1320440625/fullpdf
Reference24 articles.
1. The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate Sulfatase
2. Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status
3. Full expression of Hunter's disease in a female with an X-chromosome deletion leading to non-random inactivation
4. Duchenne muscular dystrophy in one of monozygotic twin girls.
5. Monozygotic female twin carriers discordant for the clinical manifestations of Duchenne muscular dystrophy
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