4q35

A chromosome band present on 4q
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Repetitive sequences account for more than 50% of the human genome. Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal… (More)
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Highly Cited
2010
Highly Cited
2010
Facioscapulohumeral muscular dystrophy (FSHD) is a common form of muscular dystrophy in adults that is foremost characterized by… (More)
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Highly Cited
2007
Highly Cited
2007
Autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) is mainly characterized by progressive wasting and weakness of… (More)
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Highly Cited
2007
Highly Cited
2007
Facioscapulohumeral muscular dystrophy (FSHD) patients carry contractions of the D4Z4-tandem repeat array on chromosome 4q35… (More)
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Highly Cited
2006
Highly Cited
2006
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder that is not due to a classical… (More)
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Highly Cited
2002
Highly Cited
2002
Facioscapulohumeral muscular dystrophy (FSHD), a common myopathy, is an autosomal dominant disease of unknown molecular mechanism… (More)
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Highly Cited
1999
Highly Cited
1999
Genotype analysis by using the p13E-11 probe and other 4q35 polymorphic markers was performed in 122 Italian facioscapulohumeral… (More)
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1998
1998
Bipolar affective disorder (BAD) affects approximately 1% of the population and shows strong heritability. To identify potential… (More)
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Highly Cited
1995
Highly Cited
1995
In facioscapulohumeral muscular dystrophy (FSHD), the wide range of clinical severity observed both within and between families… (More)
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Highly Cited
1992
Highly Cited
1992
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder which maps to chromosome 4qter… (More)
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