Rare novel variants in the ZIC3 gene cause X-linked heterotaxy

Aimee D. C. Paulussen; Anja Steyls; Jo Vanoevelen; Florence H. J. van Tienen; Ingrid P. C. Krapels; Godelieve R. F. Claes; Sonja Chocron; Crool Velter; Gita M. Tan-Sindhunata; Catarina Lundin; Irene Valenzuela; Balint Nagy; Iben Bache; Lisa Leth Maroun; Kristiina Avela; Han G. Brunner; Hubert J. M. Smeets; Jeroen Bakkers; Arthur van den Wijngaard

doi:10.1038/ejhg.2016.91

Rare novel variants in the ZIC3 gene cause X-linked heterotaxy

Aimee D. C. Paulussen, Anja Steyls, Jo Vanoevelen, Florence H. J. van Tienen, Ingrid P. C. Krapels, Godelieve R. F. Claes, Sonja Chocron, Crool Velter, Gita M. Tan-Sindhunata, Catarina Lundin, Irene Valenzuela, Balint Nagy, Iben Bache, Lisa Leth Maroun, Kristiina Avela, Han G. Brunner, Hubert J. M. Smeets, Jeroen Bakkers, Arthur van den Wijngaard

Clinicum

Tutkimustuotos: Artikkelijulkaisu › Artikkeli › Tieteellinen › vertaisarvioitu

Alkuperäiskieli	englanti
Lehti	European Journal of Human Genetics
Vuosikerta	24
Numero	12
Sivut	1783-1791
Sivumäärä	9
ISSN	1018-4813
DOI - pysyväislinkit	https://doi.org/10.1038/ejhg.2016.91
Tila	Julkaistu - jouluk. 2016
OKM-julkaisutyyppi	A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä, vertaisarvioitu

Tieteenalat

3111 Biolääketieteet
1182 Biokemia, solu- ja molekyylibiologia

Pääsy asiakirjaan

10.1038/ejhg.2016.91

Siteeraa tätä

Paulussen, A. D. C., Steyls, A., Vanoevelen, J., van Tienen, F. H. J., Krapels, I. P. C., Claes, G. R. F., Chocron, S., Velter, C., Tan-Sindhunata, G. M., Lundin, C., Valenzuela, I., Nagy, B., Bache, I., Maroun, L. L., Avela, K., Brunner, H. G., Smeets, H. J. M., Bakkers, J., & van den Wijngaard, A. (2016). Rare novel variants in the ZIC3 gene cause X-linked heterotaxy. European Journal of Human Genetics, 24(12), 1783-1791. https://doi.org/10.1038/ejhg.2016.91

@article{eadc7843beb04087b0d33aea54c5f25c,

title = "Rare novel variants in the ZIC3 gene cause X-linked heterotaxy",

keywords = "CONGENITAL HEART-DISEASE, OUTLET RIGHT VENTRICLE, RIGHT ATRIAL ISOMERISM, LEFT-RIGHT ASYMMETRY, LEFT-RIGHT AXIS, GREAT-ARTERIES, SITUS ABNORMALITIES, CARDIAC DEVELOPMENT, MUTATIONS, ZEBRAFISH, 3111 Biomedicine, 1182 Biochemistry, cell and molecular biology",

author = "Paulussen, {Aimee D. C.} and Anja Steyls and Jo Vanoevelen and {van Tienen}, {Florence H. J.} and Krapels, {Ingrid P. C.} and Claes, {Godelieve R. F.} and Sonja Chocron and Crool Velter and Tan-Sindhunata, {Gita M.} and Catarina Lundin and Irene Valenzuela and Balint Nagy and Iben Bache and Maroun, {Lisa Leth} and Kristiina Avela and Brunner, {Han G.} and Smeets, {Hubert J. M.} and Jeroen Bakkers and {van den Wijngaard}, Arthur",

year = "2016",

month = dec,

doi = "10.1038/ejhg.2016.91",

language = "English",

volume = "24",

pages = "1783--1791",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Springer",

number = "12",

}

Paulussen, ADC, Steyls, A, Vanoevelen, J, van Tienen, FHJ, Krapels, IPC, Claes, GRF, Chocron, S, Velter, C, Tan-Sindhunata, GM, Lundin, C, Valenzuela, I, Nagy, B, Bache, I, Maroun, LL, Avela, K, Brunner, HG, Smeets, HJM, Bakkers, J & van den Wijngaard, A 2016, 'Rare novel variants in the ZIC3 gene cause X-linked heterotaxy', European Journal of Human Genetics, Vuosikerta 24, Nro 12, Sivut 1783-1791. https://doi.org/10.1038/ejhg.2016.91

TY - JOUR

T1 - Rare novel variants in the ZIC3 gene cause X-linked heterotaxy

AU - Paulussen, Aimee D. C.

AU - Steyls, Anja

AU - Vanoevelen, Jo

AU - van Tienen, Florence H. J.

AU - Krapels, Ingrid P. C.

AU - Claes, Godelieve R. F.

AU - Chocron, Sonja

AU - Velter, Crool

AU - Tan-Sindhunata, Gita M.

AU - Lundin, Catarina

AU - Valenzuela, Irene

AU - Nagy, Balint

AU - Bache, Iben

AU - Maroun, Lisa Leth

AU - Avela, Kristiina

AU - Brunner, Han G.

AU - Smeets, Hubert J. M.

AU - Bakkers, Jeroen

AU - van den Wijngaard, Arthur

PY - 2016/12

Y1 - 2016/12

KW - CONGENITAL HEART-DISEASE

KW - OUTLET RIGHT VENTRICLE

KW - RIGHT ATRIAL ISOMERISM

KW - LEFT-RIGHT ASYMMETRY

KW - LEFT-RIGHT AXIS

KW - GREAT-ARTERIES

KW - SITUS ABNORMALITIES

KW - CARDIAC DEVELOPMENT

KW - MUTATIONS

KW - ZEBRAFISH

KW - 3111 Biomedicine

KW - 1182 Biochemistry, cell and molecular biology

U2 - 10.1038/ejhg.2016.91

DO - 10.1038/ejhg.2016.91

M3 - Article

SN - 1018-4813

VL - 24

SP - 1783

EP - 1791

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 12

ER -