Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings

E.A. Croonen; W.M. Nillesen; K.E. Stuurman; G. Oudesluijs; I.M.B.M. van de Laar; L. Martens; C. Ockeloen; I.B. Mathijssen; M. Schepens; M. Ruiterkamp-Versteeg; H. Scheffer; B.H.W. Faas; I. van der Burgt; H.G. Yntema

doi:10.1038/ejhg.2012.285

Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings

E.A. Croonen, W.M. Nillesen, K.E. Stuurman, G. Oudesluijs, I.M.B.M. van de Laar, L. Martens, C. Ockeloen, I.B. Mathijssen, M. Schepens, M. Ruiterkamp-Versteeg, H. Scheffer, B.H.W. Faas, I. van der Burgt, H.G. Yntema

Clinical genetics

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

Original language	Undefined/Unknown
Pages (from-to)	936-942
Journal	European Journal of Human Genetics
Volume	21
Issue number	9
DOIs	https://doi.org/10.1038/ejhg.2012.285
Publication status	Published - 2013

Access to Document

10.1038/ejhg.2012.285

Cite this

Croonen, E. A., Nillesen, W. M., Stuurman, K. E., Oudesluijs, G., van de Laar, I. M. B. M., Martens, L., Ockeloen, C., Mathijssen, I. B., Schepens, M., Ruiterkamp-Versteeg, M., Scheffer, H., Faas, B. H. W., van der Burgt, I., & Yntema, H. G. (2013). Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings. European Journal of Human Genetics, 21(9), 936-942. https://doi.org/10.1038/ejhg.2012.285

Croonen, E.A. ; Nillesen, W.M. ; Stuurman, K.E. ; Oudesluijs, G. ; van de Laar, I.M.B.M. ; Martens, L. ; Ockeloen, C. ; Mathijssen, I.B. ; Schepens, M. ; Ruiterkamp-Versteeg, M. ; Scheffer, H. ; Faas, B.H.W. ; van der Burgt, I. ; Yntema, H.G. / Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings. In: European Journal of Human Genetics. 2013 ; Vol. 21, No. 9. pp. 936-942.

@article{6b221ef1dfc5479197ccdd08efe2ca21,

title = "Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings",

author = "E.A. Croonen and W.M. Nillesen and K.E. Stuurman and G. Oudesluijs and {van de Laar}, I.M.B.M. and L. Martens and C. Ockeloen and I.B. Mathijssen and M. Schepens and M. Ruiterkamp-Versteeg and H. Scheffer and B.H.W. Faas and {van der Burgt}, I. and H.G. Yntema",

year = "2013",

doi = "10.1038/ejhg.2012.285",

language = "Undefined/Unknown",

volume = "21",

pages = "936--942",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

number = "9",

}

Croonen, EA, Nillesen, WM, Stuurman, KE, Oudesluijs, G, van de Laar, IMBM, Martens, L, Ockeloen, C, Mathijssen, IB, Schepens, M, Ruiterkamp-Versteeg, M, Scheffer, H, Faas, BHW, van der Burgt, I & Yntema, HG 2013, 'Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings', European Journal of Human Genetics, vol. 21, no. 9, pp. 936-942. https://doi.org/10.1038/ejhg.2012.285

Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings. / Croonen, E.A.; Nillesen, W.M.; Stuurman, K.E.; Oudesluijs, G.; van de Laar, I.M.B.M.; Martens, L.; Ockeloen, C.; Mathijssen, I.B.; Schepens, M.; Ruiterkamp-Versteeg, M.; Scheffer, H.; Faas, B.H.W.; van der Burgt, I.; Yntema, H.G.

In: European Journal of Human Genetics, Vol. 21, No. 9, 2013, p. 936-942.

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

TY - JOUR

T1 - Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings

AU - Croonen, E.A.

AU - Nillesen, W.M.

AU - Stuurman, K.E.

AU - Oudesluijs, G.

AU - van de Laar, I.M.B.M.

AU - Martens, L.

AU - Ockeloen, C.

AU - Mathijssen, I.B.

AU - Schepens, M.

AU - Ruiterkamp-Versteeg, M.

AU - Scheffer, H.

AU - Faas, B.H.W.

AU - van der Burgt, I.

AU - Yntema, H.G.

PY - 2013

Y1 - 2013

U2 - 10.1038/ejhg.2012.285

DO - 10.1038/ejhg.2012.285

M3 - Article

C2 - 23321623

VL - 21

SP - 936

EP - 942

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

IS - 9

ER -