(Q37894618)

24 August 2017

1 reference

title

Targeted ultrasound examination and DNA testing for Noonan syndrome, in fetuses with increased nuchal translucency and normal karyotype (English)

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24 August 2017

0 references

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1

M Bakker

1 reference

24 August 2017

E Pajkrt

2

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24 August 2017

I B Mathijssen

series ordinal

3

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24 August 2017

C M Bilardo

series ordinal

4

1 reference

24 August 2017

language of work or name

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27 June 2011

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24 August 2017

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24 August 2017

volume

31

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24 August 2017

issue

9

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24 August 2017

page(s)

833-840

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Noonan syndrome: a cryptic condition in early gestation.

24 August 2017

cites work

1 reference

Increased nuchal translucency thickness and normal karyotype: time for parental reassurance.

21 January 2018

1 reference

Persistent right umbilical vein in a fetus with Noonan's syndrome: a case report

21 January 2018

1 reference

Outcome of chromosomally normal livebirths with increased fetal nuchal translucency at 10-14 weeks' gestation

21 January 2018

1 reference

Noonan syndrome: diagnostic difficulties. A case report and literature review

21 January 2018

1 reference

Noonan syndrome: prenatal diagnosis in a woman carrying a PTPN11 gene mutation

21 January 2018

1 reference

Fetal nuchal translucency and normal chromosomes: a long-term follow-up study.

21 January 2018

1 reference

Noonan syndrome and related disorders: a review of clinical features and mutations in genes of the RAS/MAPK pathway.

21 January 2018

1 reference

Spontaneous resolution of cystic hygroma and hydrops in a fetus with Noonan's syndrome.

21 January 2018

1 reference

PTPN11 analysis for the prenatal diagnosis of Noonan syndrome in fetuses with abnormal ultrasound findings

21 January 2018

1 reference

Poor prenatal detection rate of cardiac anomalies in Noonan syndrome

21 January 2018

1 reference

Prenatal features of Noonan syndrome

21 January 2018

1 reference

Noonan syndrome. An update and review for the primary pediatrician

21 January 2018

1 reference

Prenatal DNA diagnosis of Noonan syndrome in a fetus with massive hygroma colli, pleural effusion and ascites

21 January 2018

1 reference

Hyperactive Ras in developmental disorders and cancer

21 January 2018

1 reference

Long-term outcome of children born after a first-trimester measurement of nuchal translucency at the 99th percentile or greater with normal karyotype: a prospective study

21 January 2018

1 reference

A clinical study of Noonan syndrome

21 January 2018

1 reference

Increased nuchal translucency with normal karyotype

21 January 2018

1 reference

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

21 January 2018

1 reference

PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity

21 January 2018

1 reference

Lymphedema in Noonan syndrome: clues to pathogenesis and prenatal diagnosis and review of the literature

21 January 2018

1 reference

UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10–14 weeks of gestation

21 January 2018

1 reference

Early fetal death associated with compound heterozygosity for Noonan syndrome-causativePTPN11 mutations

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PD.2782

1 reference

24 August 2017

1 reference