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17q11.1

A chromosome band present on 17q
National Institutes of Health

Papers overview

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2018
2018
Neuroblastoma, the most common solid tumour in early childhood, is characterized by very frequent chromosomal copy number… Expand
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2010
2010
Purpose: Several prognostic gene expression profiles have been identified in breast cancer. In spite of this progress in… Expand
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2010
2010
OBJECTIVE Prenatal diagnosis of small supernumerary marker chromosomes (sSMC) gives rise to difficulties in genetic counseling… Expand
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2009
2009
As research in developmental and clinical sciences has progressed in the last decades, there have been many important… Expand
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2006
2006
Gain of chromosome 17 is the most prevalent genetic abnormality identified in neuroblastoma (NB) and distal 17q gain has… Expand
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2003
2003
Congenital cataracts are an important cause of blindness worldwide. In a family of Chinese descent, a dominant congenital nuclear… Expand
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Highly Cited
2000
Highly Cited
2000
PURPOSE To map the locus for autosomal dominant cataracts (ADCs) in a Brazilian family using candidate gene linkage analyses… Expand
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1998
1998
BACKGROUND The serotonin transporter (5-HTT) is an important candidate gene for the genetic transmission of manic depressive… Expand
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1997
1997
Bleomycin hydrolase (BH) is the only known eukaryotic enzyme that inactivates the widely used antineoplastic agent bleomycin (BLM… Expand
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Highly Cited
1993
Highly Cited
1993
A Na(+)- and Cl(-)-coupled serotonin (5-hydroxytryptamine, 5HT) transporter is expressed on human neuronal, platelet, placental… Expand
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