9q34

A chromosome band present on 9q
National Institutes of Health

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Highly Cited
2009
Highly Cited
2009
We conducted a two-stage genome-wide association study of pancreatic cancer, a cancer with one of the lowest survival rates… (More)
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Highly Cited
2008
Highly Cited
2008
Tuberous sclerosis is a single-gene disorder caused by heterozygous mutations in the TSC1 (9q34) or TSC2 (16p13.3) gene and is… (More)
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Highly Cited
2006
Highly Cited
2006
A clinically recognizable 9q subtelomeric deletion syndrome has recently been established. Common features seen in these patients… (More)
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Highly Cited
2004
Highly Cited
2004
Juvenile amyotrophic lateral sclerosis (ALS4) is a rare autosomal dominant form of juvenile amyotrophic lateral sclerosis (ALS… (More)
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Highly Cited
2002
Highly Cited
2002
Congenital generalized lipodystrophy is an autosomal recessive disorder characterized by marked paucity of adipose tissue… (More)
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Highly Cited
2001
Highly Cited
2001
Thrombotic thrombocytopenic purpura (TTP) is a life-threatening systemic illness of abrupt onset and unknown cause. Proteolysis… (More)
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1999
1999
Deletions involving chromosome 9 occur in more than 50% of human bladder cancers of all grades and stages. Most involve loss of… (More)
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Highly Cited
1998
Highly Cited
1998
We performed genetic mapping studies of an 11-generation pedigree with an autosomal dominant, juvenile-onset motor-systems… (More)
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Highly Cited
1997
Highly Cited
1997
Early-onset torsion dystonia is a movement disorder, characterized by twisting muscle contractures, that begins in childhood… (More)
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1983
1983
Phenotypic, karyotypic, and developmental homology between affected children of carriers of an inverted insertion (9) (q22.1q34… (More)
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