9p13

A chromosome band present on 9p
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
Chronic lymphocytic leukaemia (CLL) is a frequent disease in which the genetic alterations determining the clinicobiological… (More)
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Highly Cited
2005
Highly Cited
2005
Primary muscle coenzyme Q10 (CoQ10) deficiency is an apparently autosomal recessive condition with heterogeneous clinical… (More)
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Highly Cited
2003
Highly Cited
2003
Preeclampsia is a common, pregnancy-specific disorder characterized by reduced placental perfusion, endothelial dysfunction… (More)
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Highly Cited
2001
Highly Cited
2001
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative disease among Europeans and people of European… (More)
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2000
2000
Papillary renal cell carcinomas (RCCs) have characteristic clinical and morphological features that separate them from the more… (More)
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Highly Cited
1998
Highly Cited
1998
Fanconi anemia (FA) is an autosomal recessive disease with diverse clinical symptoms including developmental anomalies, bone… (More)
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Highly Cited
1998
Highly Cited
1998
Secondary Lymphoid-tissue Chemokine (SLC) is a recently identified CC chemokine that is constitutively expressed in various… (More)
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Highly Cited
1997
Highly Cited
1997
By searching the Expressed Sequence Tag (EST) data base, we identified partial cDNA sequences potentially encoding a novel human… (More)
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Highly Cited
1997
Highly Cited
1997
By searching the expressed sequence tag (EST) data base, we identified partial cDNA sequences encoding a novel human CC chemokine… (More)
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Highly Cited
1996
Highly Cited
1996
The t(9;14)(p13;q32) translocation is associated with approximately 50% of lymphoplasmacytoid lymphoma (LPL), a subtype of B-cell… (More)
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