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17q11.1

A chromosome band present on 17q
National Institutes of Health

Papers overview

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2018
2018
ABSTRACT Neuroblastoma, the most common solid tumour in early childhood, is characterized by very frequent chromosomal copy… Expand
Highly Cited
2010
Highly Cited
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
2006
2006
Gain of chromosome 17 is the most prevalent genetic abnormality identified in neuroblastoma (NB) and distal 17q gain has… Expand
Highly Cited
2003
Highly Cited
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
Highly Cited
1998
Highly Cited
1998
BACKGROUND The serotonin transporter (5-HTT) is an important candidate gene for the genetic transmission of manic depressive… Expand
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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