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

Onderzoeksoutput: Bijdrage aan tijdschrift › Artikel › peer review

Originele taal-2	Engels
Pagina's (van-tot)	242-6
Aantal pagina's	5
Tijdschrift	Leukemia
Volume	24
Nummer van het tijdschrift	1
DOI's	https://doi.org/10.1038/leu.2009.210
Status	Gepubliceerd - jan. 2010
Extern gepubliceerd	Ja

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10.1038/leu.2009.210

Citeer dit

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

@article{76d94e3a2d61427b842832860a27ce60,

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

keywords = "Blood Platelet Disorders/diagnosis, Child, Child, Preschool, Core Binding Factor Alpha 2 Subunit/genetics, Female, Gene Deletion, Humans, Leukemia, Myeloid, Acute/diagnosis, Male, Mutation",

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",

language = "English",

volume = "24",

pages = "242--6",

journal = "Leukemia",

issn = "0887-6924",

number = "1",

}

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, nr. 1, blz. 242-6. https://doi.org/10.1038/leu.2009.210

TY - JOUR

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/diagnosis

KW - Child

KW - Child, Preschool

KW - Core Binding Factor Alpha 2 Subunit/genetics

KW - Female

KW - Gene Deletion

KW - Humans

KW - Leukemia, Myeloid, Acute/diagnosis

KW - Male

KW - Mutation

U2 - 10.1038/leu.2009.210

DO - 10.1038/leu.2009.210

M3 - Article

C2 - 19946261

VL - 24

SP - 242

EP - 246

JO - Leukemia

JF - Leukemia

SN - 0887-6924

IS - 1

ER -