(Q37310945)

English

Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literature

scientific article published on 29 October 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

1 reference

Europe PubMed Central

Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literature (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

Noonan syndrome

1 reference

based on heuristic

inferred from title

author name string

Fu-Sung Lo

1

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

Ju-Li Lin

2

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

Min-Tzu Kuo

3

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

Pao-Chin Chiu

4

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

San-Ging Shu

5

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

Mei-Chyn Chao

6

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

Yann-Jinn Lee

7

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

Shuan-Pei Lin

8

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

publication date

29 October 2008

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

168

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Europe PubMed Central

PubMed publication ID

19 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

919-923

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

What's new in the neuro-cardio-facial-cutaneous syndromes?

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline KRAS mutations cause Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further evidence of genetic heterogeneity in Costello syndrome: involvement of the KRAS gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype-phenotype relationships and overlap with Costello syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumor development in three patients with Noonan syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of PTPN11 gene in Taiwanese children with Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype-phenotype correlations in Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline mutations in HRAS proto-oncogene cause Costello syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An unexpected new role of mutant Ras: perturbation of human embryonic development

1 reference

https://pubmed.ncbi.nlm.nih.gov/18958496

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-008-0858-Z

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 August 2017

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