(Q51861421)

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title

Prenatal features of Noonan syndrome: prevalence and prognostic value. (English)

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2

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Marco Tartaglia

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Margherita Cirillo Silengo

9

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author name string

G Baldassarre

1

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A Dotta

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E Banaudi

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S Forzano

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A Marinosci

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C Rossi

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G B Ferrero

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publication date

11 July 2011

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published in

Prenatal Diagnosis

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volume

31

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issue

10

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page(s)

949-954

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Noonan syndrome: a cryptic condition in early gestation.

cites work

1 reference

Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype

21 January 2018

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A restricted spectrum of NRAS mutations causes Noonan syndrome

21 January 2018

1 reference

Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair

21 January 2018

1 reference

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

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

Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype.

21 January 2018

1 reference

Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia

21 January 2018

1 reference

Prenatal features of Noonan syndrome

21 January 2018

1 reference

Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy

21 January 2018

1 reference

Germline gain-of-function mutations in RAF1 cause Noonan syndrome

21 January 2018

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Germline gain-of-function mutations in SOS1 cause Noonan syndrome

21 January 2018

1 reference

Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum

21 January 2018

1 reference

A clinical study of Noonan syndrome

21 January 2018

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

21 January 2018

1 reference

Germline KRAS mutations cause Noonan syndrome

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

Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.

21 January 2018

1 reference

Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PD.2804

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