Standard
Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes. / Stoltze, Ulrik Kristoffer; Hansen, Thomas Van Overeem; Brok, Jesper Sune; Gronskov, Karen; Tumer, Asuman Z.; Ahlborn, Lise Barlebo; Schmiegelow, Kjeld; Wadt, Karin A.W.
In:
Journal of Medical Genetics, Vol. 60, No. 2, 108335, 2023, p. 128-130.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Stoltze, UK
, Hansen, TVO, Brok, JS, Gronskov, K
, Tumer, AZ, Ahlborn, LB
, Schmiegelow, K & Wadt, KAW 2023, '
Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes',
Journal of Medical Genetics, vol. 60, no. 2, 108335, pp. 128-130.
https://doi.org/10.1136/jmedgenet-2021-108335
APA
Stoltze, U. K.
, Hansen, T. V. O., Brok, J. S., Gronskov, K.
, Tumer, A. Z., Ahlborn, L. B.
, Schmiegelow, K., & Wadt, K. A. W. (2023).
Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes.
Journal of Medical Genetics,
60(2), 128-130. [108335].
https://doi.org/10.1136/jmedgenet-2021-108335
Vancouver
Stoltze UK
, Hansen TVO, Brok JS, Gronskov K
, Tumer AZ, Ahlborn LB et al.
Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes.
Journal of Medical Genetics. 2023;60(2):128-130. 108335.
https://doi.org/10.1136/jmedgenet-2021-108335
Author
Stoltze, Ulrik Kristoffer ; Hansen, Thomas Van Overeem ; Brok, Jesper Sune ; Gronskov, Karen ; Tumer, Asuman Z. ; Ahlborn, Lise Barlebo ; Schmiegelow, Kjeld ; Wadt, Karin A.W. / Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes. In: Journal of Medical Genetics. 2023 ; Vol. 60, No. 2. pp. 128-130.
Bibtex
@article{f4982f4d56394e0cb9ba931e7b70ca3a,
title = "Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes",
keywords = "epigenomics, genomics, medical oncology, pediatrics, sequence deletion",
author = "Stoltze, {Ulrik Kristoffer} and Hansen, {Thomas Van Overeem} and Brok, {Jesper Sune} and Karen Gronskov and Tumer, {Asuman Z.} and Ahlborn, {Lise Barlebo} and Kjeld Schmiegelow and Wadt, {Karin A.W.}",
note = "Funding Information: Funding was received from B{\o}rneCancerFonden, the European Regional Development fund (Interregional Childhood Oncology Precision Medicine Exploration (iCOPE). This work is part of Childhood Oncology Network Targeting Research, Organisation & Life expectancy (CONTROL) and supported by Danish Cancer Society (R-257-A14720) and the Danish Childhood Cancer Foundation (2019-5934). ",
year = "2023",
doi = "10.1136/jmedgenet-2021-108335",
language = "English",
volume = "60",
pages = "128--130",
journal = "Journal of Medical Genetics",
issn = "0022-2593",
publisher = "B M J Group",
number = "2",
}
RIS
TY - JOUR
T1 - Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes
AU - Stoltze, Ulrik Kristoffer
AU - Hansen, Thomas Van Overeem
AU - Brok, Jesper Sune
AU - Gronskov, Karen
AU - Tumer, Asuman Z.
AU - Ahlborn, Lise Barlebo
AU - Schmiegelow, Kjeld
AU - Wadt, Karin A.W.
N1 - Funding Information:
Funding was received from BørneCancerFonden, the European Regional Development fund (Interregional Childhood Oncology Precision Medicine Exploration (iCOPE). This work is part of Childhood Oncology Network Targeting Research, Organisation & Life expectancy (CONTROL) and supported by Danish Cancer Society (R-257-A14720) and the Danish Childhood Cancer Foundation (2019-5934).
PY - 2023
Y1 - 2023
KW - epigenomics
KW - genomics
KW - medical oncology
KW - pediatrics
KW - sequence deletion
U2 - 10.1136/jmedgenet-2021-108335
DO - 10.1136/jmedgenet-2021-108335
M3 - Journal article
C2 - 35772845
AN - SCOPUS:85134684986
VL - 60
SP - 128
EP - 130
JO - Journal of Medical Genetics
JF - Journal of Medical Genetics
SN - 0022-2593
IS - 2
M1 - 108335
ER -