Implementing fast whole exome sequencing sequencing as diagnostic test for fetal multiple congenital anomalies on ultrasound

N. Corsten-Janssen; J. el Mecky; K. Bouman; Y. J. Vos; J. B. G. M. Verheij; H. Westers; R. Kinds; A. J. Scheper; B. Sikkema-Raddatz; R. J. Sinke; I. M. van Langen; R. H. Sijmons; C. C. van Diemen

Implementing fast whole exome sequencing sequencing as diagnostic test for fetal multiple congenital anomalies on ultrasound

N. Corsten-Janssen, J. el Mecky, K. Bouman, Y. J. Vos, J. B. G. M. Verheij, H. Westers, R. Kinds, A. J. Scheper, B. Sikkema-Raddatz, R. J. Sinke, I. M. van Langen, R. H. Sijmons, C. C. van Diemen

Health Psychology Research (HPR)

Research output: Contribution to journal › Meeting Abstract › Academic

Original language	English
Pages (from-to)	540-540
Number of pages	1
Journal	European Journal of Human Genetics
Volume	27
Publication status	Published - Jul-2019
Event	51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) - Milan, Italy Duration: 16-Jun-2018 → 19-Jun-2018

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Corsten-Janssen, N., el Mecky, J., Bouman, K., Vos, Y. J., Verheij, J. B. G. M., Westers, H., Kinds, R., Scheper, A. J., Sikkema-Raddatz, B., Sinke, R. J., van Langen, I. M., Sijmons, R. H., & van Diemen, C. C. (2019). Implementing fast whole exome sequencing sequencing as diagnostic test for fetal multiple congenital anomalies on ultrasound. European Journal of Human Genetics, 27, 540-540.

@article{c8b732752fd34455ac55fb91942e13de,

title = "Implementing fast whole exome sequencing sequencing as diagnostic test for fetal multiple congenital anomalies on ultrasound",

author = "N. Corsten-Janssen and {el Mecky}, J. and K. Bouman and Vos, {Y. J.} and Verheij, {J. B. G. M.} and H. Westers and R. Kinds and Scheper, {A. J.} and B. Sikkema-Raddatz and Sinke, {R. J.} and {van Langen}, {I. M.} and Sijmons, {R. H.} and {van Diemen}, {C. C.}",

year = "2019",

month = jul,

language = "English",

volume = "27",

pages = "540--540",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

note = "51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) ; Conference date: 16-06-2018 Through 19-06-2018",

}

Corsten-Janssen, N, el Mecky, J, Bouman, K, Vos, YJ, Verheij, JBGM , Westers, H, Kinds, R, Scheper, AJ, Sikkema-Raddatz, B, Sinke, RJ, van Langen, IM, Sijmons, RH & van Diemen, CC 2019, 'Implementing fast whole exome sequencing sequencing as diagnostic test for fetal multiple congenital anomalies on ultrasound', European Journal of Human Genetics, vol. 27, pp. 540-540.

TY - JOUR

T1 - Implementing fast whole exome sequencing sequencing as diagnostic test for fetal multiple congenital anomalies on ultrasound

AU - Corsten-Janssen, N.

AU - el Mecky, J.

AU - Bouman, K.

AU - Vos, Y. J.

AU - Verheij, J. B. G. M.

AU - Westers, H.

AU - Kinds, R.

AU - Scheper, A. J.

AU - Sikkema-Raddatz, B.

AU - Sinke, R. J.

AU - van Langen, I. M.

AU - Sijmons, R. H.

AU - van Diemen, C. C.

PY - 2019/7

Y1 - 2019/7

M3 - Meeting Abstract

SN - 1018-4813

VL - 27

SP - 540

EP - 540

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

T2 - 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)

Y2 - 16 June 2018 through 19 June 2018

ER -