SF3B1 mutations correlated to cytogenetics and mutations in NOTCH1, FBXW7, MYD88, XPO1 and TP53 in 1160 untreated CLL patients. (Q52644149)

5 May 2018

title

SF3B1 mutations correlated to cytogenetics and mutations in NOTCH1, FBXW7, MYD88, XPO1 and TP53 in 1160 untreated CLL patients. (English)

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5 May 2018

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10

T Haferlach

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3

C Haferlach

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12

S Schnittger

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5 May 2018

author name string

S Jeromin

1

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5 May 2018

S Weissmann

2

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F Dicker

4

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K Bayer

5

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V Grossmann

6

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T Alpermann

7

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A Roller

8

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A Kohlmann

9

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5 May 2018

W Kern

11

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publication date

12 September 2013

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5 May 2018

published in

Leukemia

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5 May 2018

volume

28

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5 May 2018

issue

1

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5 May 2018

page(s)

108-117

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https://scigraph.springernature.com/pub.10.1038/leu.2013.263

exact match

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cites work

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The detection of TP53 mutations in chronic lymphocytic leukemia independently predicts rapid disease progression and is highly correlated with a complex aberrant karyotype

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NOTCH1 mutations identify a genetic subgroup of chronic lymphocytic leukemia patients with high risk of transformation and poor outcome.

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Immunostimulatory oligonucleotide-induced metaphase cytogenetics detect chromosomal aberrations in 80% of CLL patients: A study of 132 CLL cases with correlation to FISH, IgVH status, and CD38 expression

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Identifiers

DOI

10.1038/LEU.2013.263

1 reference

5 May 2018

PubMed ID

24113472

1 reference

5 May 2018