(Q44791863)

6 December 2017

Mutations in PTPN11 are uncommon in adult myelodysplastic syndromes and acute myeloid leukaemia (English)

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6 December 2017

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4

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6 December 2017

Johan MF

1

1 reference

6 December 2017

Bowen DT

2

1 reference

6 December 2017

Frew ME

3

1 reference

6 December 2017

Wilson GA

5

1 reference

6 December 2017

Peake IR

6

1 reference

6 December 2017

Reilly JT

7

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6 December 2017

language of work or name

English

0 references

publication date

1 March 2004

1 reference

British Journal of Haematology

6 December 2017

1 reference

6 December 2017

124

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6 December 2017

843-844

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6 December 2017

6

1 reference

Regulation of the mitogen-activated protein kinase signaling pathway by SHP2.

6 December 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2004.04862.X

Structure and function of SH2-domain containing tyrosine phosphatases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2004.04862.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2004.04862.X

Exclusion of PTPN11 mutations in Costello syndrome: further evidence for distinct genetic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2004.04862.X

10.1111/J.1365-2141.2004.04862.X

21 January 2018

Identifiers

DOI

1 reference

6 December 2017

1 reference