Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes

A. C. Houweling; Y. M. De Mooij; I. Van Der Burgt; H. G. Yntema; A. M.A. Lachmeijer; A. T.J.I. Go

doi:10.1002/pd.2458

Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes

A. C. Houweling^*
, Y. M. De Mooij
, I. Van Der Burgt
, H. G. Yntema
, A. M.A. Lachmeijer
, A. T.J.I. Go

^*Corresponding author for this work

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

Original language	English
Pages (from-to)	284-286
Number of pages	3
Journal	Prenatal Diagnosis
Volume	30
Issue number	3
DOIs	https://doi.org/10.1002/pd.2458
Publication status	Published - Mar 2010
Externally published	Yes

Keywords

KRAS
Noonan syndrome
Nuchal translucency
Prenatal
PTPN11

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10.1002/pd.2458

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@article{2485628d2b2744a5a3ee3729d38dd46f,

title = "Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes",

keywords = "KRAS, Noonan syndrome, Nuchal translucency, Prenatal, PTPN11",

author = "Houweling, \{A. C.\} and \{De Mooij\}, \{Y. M.\} and \{Van Der Burgt\}, I. and Yntema, \{H. G.\} and Lachmeijer, \{A. M.A.\} and Go, \{A. T.J.I.\}",

year = "2010",

month = mar,

doi = "10.1002/pd.2458",

language = "English",

volume = "30",

pages = "284--286",

journal = "Prenatal Diagnosis",

issn = "0197-3851",

publisher = "John Wiley \& Sons Inc.",

number = "3",

}

TY - JOUR

T1 - Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes

AU - Houweling, A. C.

AU - De Mooij, Y. M.

AU - Van Der Burgt, I.

AU - Yntema, H. G.

AU - Lachmeijer, A. M.A.

AU - Go, A. T.J.I.

PY - 2010/3

Y1 - 2010/3

KW - KRAS

KW - Noonan syndrome

KW - Nuchal translucency

KW - Prenatal

KW - PTPN11

UR - https://www.scopus.com/pages/publications/77349112965

U2 - 10.1002/pd.2458

DO - 10.1002/pd.2458

M3 - Article

C2 - 20112233

AN - SCOPUS:77349112965

SN - 0197-3851

VL - 30

SP - 284

EP - 286

JO - Prenatal Diagnosis

JF - Prenatal Diagnosis

IS - 3

ER -

Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes

Keywords

Access to Document

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