(Q37385200)

20 August 2017

Genotype differences in cognitive functioning in Noonan syndrome (English)

1 reference

20 August 2017

1 reference

E I Pierpont

1

1 reference

20 August 2017

M E Pierpont

2

1 reference

20 August 2017

N J Mendelsohn

3

1 reference

20 August 2017

A E Roberts

4

1 reference

20 August 2017

E Tworog-Dube

5

1 reference

20 August 2017

M S Seidenberg

6

1 reference

20 August 2017

language of work or name

English

0 references

publication date

11 December 2008

1 reference

Genes, Brain and Behavior

20 August 2017

1 reference

20 August 2017

8

1 reference

20 August 2017

3

1 reference

20 August 2017

275-282

1 reference

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

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Control of CNS cell-fate decisions by SHP-2 and its dysregulation in Noonan syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Deregulated Ras signaling in developmental disorders: new tricks for an old dog.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Psychological and cognitive functioning in children and adolescents with congenital heart disease: a meta-analysis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Germline KRAS mutations cause Noonan syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Genetic and environmental influences on vocabulary IQ: parental education level as moderator

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Noonan syndrome: a review

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Audiologic manifestations of Noonan syndrome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Noonan and cardio-facio-cutaneous syndromes: two clinically and genetically overlapping disorders.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Further delineation of cardio-facio-cutaneous syndrome: clinical features of 38 individuals with proven mutations.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Neurological complications of cardio-facio-cutaneous syndrome.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

Psychological profile of children with Noonan syndrome.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760992

The Impact of Maternal Perceptions and Medical Severity on the Adjustment of Children with Congenital Heart Disease

2 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19077116

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Clinical and molecular studies in a large Dutch family with Noonan syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19077116

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19077116

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1601-183X.2008.00469.X

1 reference

20 August 2017

1 reference

20 August 2017

1 reference