Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood: a family report on co-occurring FANCC and CHEK2 mutations

Gerbrig Berger; Eva van den Berg; Stephanie Smetsers; Beike K Leegte; Rolf H Sijmons; Kristin M Abbott; André B Mulder; Edo Vellenga

doi:10.1111/bjh.15265

Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood: a family report on co-occurring FANCC and CHEK2 mutations

Gerbrig Berger, Eva van den Berg, Stephanie Smetsers, Beike K Leegte, Rolf H Sijmons, Kristin M Abbott, André B Mulder, Edo Vellenga^*

^*Bijbehorende auteur voor dit werk

Onderzoeksoutput: Letter › Academic › peer review

4 Citaten (Scopus)

8 Downloads (Pure)

Originele taal-2	English
Pagina's (van-tot)	1071-1073
Aantal pagina's	3
Tijdschrift	British Journal of Haematology
Volume	184
Nummer van het tijdschrift	6
Vroegere onlinedatum	2018
DOI's	https://doi.org/10.1111/bjh.15265
Status	Published - mrt.-2019

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10.1111/bjh.15265

Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood: a family report on co‐occurring FANCC and CHEK2 mutationsFinal publisher's version, 127 KBLicentie: Taverne

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@article{f9942cacb55c42b99fc8081b5ff763cc,

title = "Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood: a family report on co-occurring FANCC and CHEK2 mutations",

keywords = "fanconi anaemia, FANCC, CHEK2, bone marrow failure, next-generation sequencing, BREAST-CANCER RISK",

author = "Gerbrig Berger and {van den Berg}, Eva and Stephanie Smetsers and Leegte, {Beike K} and Sijmons, {Rolf H} and Abbott, {Kristin M} and Mulder, {Andr{\'e} B} and Edo Vellenga",

year = "2019",

month = mar,

doi = "10.1111/bjh.15265",

language = "English",

volume = "184",

pages = "1071--1073",

journal = "British Journal of Haematology",

issn = "0007-1048",

publisher = "Wiley",

number = "6",

}

TY - JOUR

T1 - Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood

T2 - a family report on co-occurring FANCC and CHEK2 mutations

AU - Berger, Gerbrig

AU - van den Berg, Eva

AU - Smetsers, Stephanie

AU - Leegte, Beike K

AU - Sijmons, Rolf H

AU - Abbott, Kristin M

AU - Mulder, André B

AU - Vellenga, Edo

PY - 2019/3

Y1 - 2019/3

KW - fanconi anaemia

KW - FANCC

KW - CHEK2

KW - bone marrow failure

KW - next-generation sequencing

KW - BREAST-CANCER RISK

U2 - 10.1111/bjh.15265

DO - 10.1111/bjh.15265

M3 - Letter

C2 - 29767408

SN - 0007-1048

VL - 184

SP - 1071

EP - 1073

JO - British Journal of Haematology

JF - British Journal of Haematology

IS - 6

ER -