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9q32

A chromosome band present on 9q
National Institutes of Health

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Highly Cited
2006
Highly Cited
2006
Usher syndrome is an autosomal recessive condition characterized by sensorineural hearing loss, variable vestibular dysfunction… Expand
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Highly Cited
2005
Highly Cited
2005
In most cases, small-cell carcinoma of the urinary bladder is admixed with other histological types of bladder carcinoma. To… Expand
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2001
2001
Transcriptional silencing by CpG island hypermethylation of gene regulatory regions is one mechanism for inactivation of tumour… Expand
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Highly Cited
2001
Highly Cited
2001
Schizophrenia is assumed to have complex inheritance because of its high prevalence and sporadic familial transmission. Findings… Expand
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Highly Cited
1999
Highly Cited
1999
In patients with an atypical stem-cell myeloproliferative disorder with lymphoma (B or T cell), myeloid hyperplasia, and… Expand
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Highly Cited
1998
Highly Cited
1998
The NIMH Genetics Initiative is a multi-site collaborative study designed to create a national resource for genetic studies of… Expand
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Highly Cited
1997
Highly Cited
1997
A novel (TL1), a recently described (TL2) TNF-like, and three recently described TNF receptor-like (TR1, TR2, TR3) molecules were… Expand
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1997
1997
Loss of heterozygosity (LOH) on chromosome 9q is the most frequent genetic alteration in transitional cell carcinoma (TCC) of the… Expand
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1991
1991
Tuberous sclerosis (TSC) is an autosomal dominant disorder with both neurological and cutaneous manifestations often resulting in… Expand
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1990
1990
Idiopathic torsion dystonia (ITD) is a neurological disorder characterized by sustained muscle contractions that appear as… Expand
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