Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

M C J Jongmans; R P Kuiper; C L Carmichael; E J Wilkins; N Dors; A Carmagnac; A Y N Schouten-van Meeteren; X Li; M Stankovic; E Kamping; H Bengtsson; E F P M Schoenmakers; A Geurts van Kessel; P M Hoogerbrugge; C N Hahn; P P Brons; H S Scott; N Hoogerbrugge

doi:10.1038/leu.2009.210

Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

M C J Jongmans, R P Kuiper, C L Carmichael, E J Wilkins, N Dors, A Carmagnac, A Y N Schouten-van Meeteren, X Li, M Stankovic, E Kamping, H Bengtsson, E F P M Schoenmakers, A Geurts van Kessel, P M Hoogerbrugge, C N Hahn, P P Brons, H S Scott, N Hoogerbrugge

Section Oncogenetics

Research output: Contribution to journal › Article › Academic › peer-review

Original language	English
Pages (from-to)	242-6
Number of pages	5
Journal	Leukemia
Volume	24
Issue number	1
DOIs	https://doi.org/10.1038/leu.2009.210
Publication status	Published - Jan 2010

Keywords

Blood Platelet Disorders
Child
Child, Preschool
Core Binding Factor Alpha 2 Subunit
Female
Gene Deletion
Humans
Leukemia, Myeloid, Acute
Male
Mutation
Letter
Research Support, Non-U.S. Gov't

Access to Document

10.1038/leu.2009.210

Cite this

Jongmans, M. C. J., Kuiper, R. P., Carmichael, C. L., Wilkins, E. J., Dors, N., Carmagnac, A., Schouten-van Meeteren, A. Y. N., Li, X., Stankovic, M., Kamping, E., Bengtsson, H., Schoenmakers, E. F. P. M., van Kessel, A. G., Hoogerbrugge, P. M., Hahn, C. N., Brons, P. P., Scott, H. S., & Hoogerbrugge, N. (2010). Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome. Leukemia, 24(1), 242-6. https://doi.org/10.1038/leu.2009.210

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keywords = "Blood Platelet Disorders, Child, Child, Preschool, Core Binding Factor Alpha 2 Subunit, Female, Gene Deletion, Humans, Leukemia, Myeloid, Acute, Male, Mutation, Letter, Research Support, Non-U.S. Gov't",

author = "Jongmans, {M C J} and Kuiper, {R P} and Carmichael, {C L} and Wilkins, {E J} and N Dors and A Carmagnac and {Schouten-van Meeteren}, {A Y N} and X Li and M Stankovic and E Kamping and H Bengtsson and Schoenmakers, {E F P M} and {van Kessel}, {A Geurts} and Hoogerbrugge, {P M} and Hahn, {C N} and Brons, {P P} and Scott, {H S} and N Hoogerbrugge",

year = "2010",

month = jan,

doi = "10.1038/leu.2009.210",

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Jongmans, MCJ, Kuiper, RP, Carmichael, CL, Wilkins, EJ, Dors, N, Carmagnac, A, Schouten-van Meeteren, AYN, Li, X, Stankovic, M, Kamping, E, Bengtsson, H, Schoenmakers, EFPM, van Kessel, AG, Hoogerbrugge, PM, Hahn, CN, Brons, PP, Scott, HS & Hoogerbrugge, N 2010, 'Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome', Leukemia, vol. 24, no. 1, pp. 242-6. https://doi.org/10.1038/leu.2009.210

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T1 - Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia

T2 - clues for improved identification of the FPD/AML syndrome

AU - Jongmans, M C J

AU - Kuiper, R P

AU - Carmichael, C L

AU - Wilkins, E J

AU - Dors, N

AU - Carmagnac, A

AU - Schouten-van Meeteren, A Y N

AU - Li, X

AU - Stankovic, M

AU - Kamping, E

AU - Bengtsson, H

AU - Schoenmakers, E F P M

AU - van Kessel, A Geurts

AU - Hoogerbrugge, P M

AU - Hahn, C N

AU - Brons, P P

AU - Scott, H S

AU - Hoogerbrugge, N

PY - 2010/1

Y1 - 2010/1

KW - Blood Platelet Disorders

KW - Child

KW - Child, Preschool

KW - Core Binding Factor Alpha 2 Subunit

KW - Female

KW - Gene Deletion

KW - Humans

KW - Leukemia, Myeloid, Acute

KW - Male

KW - Mutation

KW - Letter

KW - Research Support, Non-U.S. Gov't

U2 - 10.1038/leu.2009.210

DO - 10.1038/leu.2009.210

M3 - Article

C2 - 19946261

SN - 0887-6924

VL - 24

SP - 242

EP - 246

JO - Leukemia

JF - Leukemia

IS - 1

ER -