The role of TBX18 in congenital heart defects in humans not confirmed

Aafke Engwerda; Kristin M. Abbott; Marrit M. Hitzert; Conny M.A. van Ravenswaaij-Arts; Wilhelmina S. Kerstjens-Frederikse

doi:10.1038/s41431-022-01242-3

The role of TBX18 in congenital heart defects in humans not confirmed

Aafke Engwerda, Kristin M. Abbott, Marrit M. Hitzert, Conny M.A. van Ravenswaaij-Arts, Wilhelmina S. Kerstjens-Frederikse^*

^*Corresponding author for this work

Clinical Cognitive Neuropsychiatry Research Program (CCNP)

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

1 Citation (Scopus)

105 Downloads (Pure)

Original language	English
Pages (from-to)	138–141
Number of pages	4
Journal	European Journal of Human Genetics
Volume	31
Early online date	22-Nov-2022
DOIs	https://doi.org/10.1038/s41431-022-01242-3
Publication status	Published - Feb-2023

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10.1038/s41431-022-01242-3

The role of TBX18 in congenital heart defects in humans not confirmedFinal publisher's version, 357 KBLicence: Taverne

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@article{082fc8b0b1d54703910a2f5acba2fba9,

title = "The role of TBX18 in congenital heart defects in humans not confirmed",

author = "Aafke Engwerda and Abbott, {Kristin M.} and Hitzert, {Marrit M.} and {van Ravenswaaij-Arts}, {Conny M.A.} and Kerstjens-Frederikse, {Wilhelmina S.}",

note = "Funding Information: This work was supported by a grant from ZonMw (113312101) and by crowdfunding organised by Chromosome 6 parents. AE is the recipient of a Junior Scientific Masterclass MD/PhD scholarship from the University Medical Center Groningen. ",

year = "2023",

month = feb,

doi = "10.1038/s41431-022-01242-3",

language = "English",

volume = "31",

pages = "138–141",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

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TY - JOUR

T1 - The role of TBX18 in congenital heart defects in humans not confirmed

AU - Engwerda, Aafke

AU - Abbott, Kristin M.

AU - Hitzert, Marrit M.

AU - van Ravenswaaij-Arts, Conny M.A.

AU - Kerstjens-Frederikse, Wilhelmina S.

N1 - Funding Information: This work was supported by a grant from ZonMw (113312101) and by crowdfunding organised by Chromosome 6 parents. AE is the recipient of a Junior Scientific Masterclass MD/PhD scholarship from the University Medical Center Groningen.

PY - 2023/2

Y1 - 2023/2

U2 - 10.1038/s41431-022-01242-3

DO - 10.1038/s41431-022-01242-3

M3 - Letter

AN - SCOPUS:85142428848

SN - 1018-4813

VL - 31

SP - 138

EP - 141

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

ER -