Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation. (Q35212696)

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25 January 2020

title

Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation (English)

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4

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Han van Krieken

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Lambertus Kiemeney

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25 January 2020

Marjolijn J L Ligtenberg

8

object named as

Marjolijn J L Ligtenberg

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5

Helger G Yntema

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25 January 2020

author name string

Marjolijn C J Jongmans

1

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Ineke van der Burgt

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25 January 2020

Peter M Hoogerbrugge

3

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Willy M Nillesen

6

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Roland P Kuiper

7

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Ad Geurts van Kessel

9

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Nicoline Hoogerbrugge

12

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language of work or name

English

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publication date

16 March 2011

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European Journal of Human Genetics

25 January 2020

published in

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volume

19

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issue

8

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25 January 2020

page(s)

870-874

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https://scigraph.springernature.com/pub.10.1038/ejhg.2011.37

25 January 2020

exact match

0 references

cites work

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Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors

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Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease

13 July 2018

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Diverse biochemical properties of Shp2 mutants. Implications for disease phenotypes

13 July 2018

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The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease

13 July 2018

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Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia

13 July 2018

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Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndrome

13 July 2018

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Activating mutations of the noonan syndrome-associated SHP2/PTPN11 gene in human solid tumors and adult acute myelogenous leukemia

13 July 2018

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Cancer risk following growth hormone use in childhood: implications for current practice

13 July 2018

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Orbital rhabdomyosarcoma in Noonan syndrome

13 July 2018

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13 July 2018

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Occurrence of myeloproliferative disorder in patients with Noonan syndrome

13 July 2018

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13 July 2018

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26 September 2018

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26 September 2018

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26 September 2018

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26 September 2018

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26 September 2018

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26 September 2018

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26 September 2018

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26 September 2018

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26 September 2018

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26 September 2018

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26 September 2018

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Genotypic and phenotypic characterization of Noonan syndrome: New data and review of the literature

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Acute lymphoblastic leukaemia in Noonan syndrome

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21 January 2018

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12 December 2020

Noonan Syndrome and Neuroblastoma

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12 December 2020

Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome

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A new NDE1/PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome

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Prevalence of priapism in children and adolescents with sickle cell anemia.

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Crossref

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7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/EJHG.2011.37

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21407260%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21407260%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

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