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17p13.1

A chromosome band present on 17p
National Institutes of Health

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Highly Cited
2016
Highly Cited
2016
BACKGROUND Irreversible inhibition of Bruton's tyrosine kinase (BTK) by ibrutinib represents an important therapeutic advance for… Expand
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Highly Cited
2015
Highly Cited
2015
BACKGROUND Patients with chronic lymphocytic leukaemia (CLL) with TP53 aberrations respond poorly to first-line… Expand
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Highly Cited
2014
Highly Cited
2014
BACKGROUND In patients with chronic lymphoid leukemia (CLL) or small lymphocytic lymphoma (SLL), a short duration of response to… Expand
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Highly Cited
2013
Highly Cited
2013
BACKGROUND The treatment of relapsed chronic lymphocytic leukemia (CLL) has resulted in few durable remissions. Bruton's tyrosine… Expand
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Highly Cited
2009
Highly Cited
2009
To determine the clinical fate of patients with de novo deletion 17p13.1 (17p-) chronic lymphocytic leukemia (CLL), we… Expand
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Highly Cited
2003
Highly Cited
2003
Nonrandom recurrent chromosomal abnormalities are ubiquitous in multiple myeloma (MM) and include, among others, translocations… Expand
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Highly Cited
2002
Highly Cited
2002
We report the identification of mutations in lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) genes in non-bullous… Expand
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Highly Cited
2000
Highly Cited
2000
Leber congenital amaurosis (LCA, MIM 204000) accounts for at least 5% of all inherited retinal disease and is the most severe… Expand
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Highly Cited
1996
Highly Cited
1996
Loss of heterozygosity (LOH) was detected in morphologically normal lobules adjacent to breast cancers. The most frequent… Expand
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Highly Cited
1996
Highly Cited
1996
Leber's congenital amaurosis (LCA, MIM 2040001), the earliest and most severe form of inherited retinopathy, accounts for at… Expand
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