(Q44153668)

30 November 2017

title

PTPN11 mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13. (English)

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30 November 2017

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30 November 2017

Maheshwari M

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30 November 2017

Fernbach S

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30 November 2017

Ho T

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30 November 2017

Molinari L

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30 November 2017

Yakub I

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30 November 2017

Yu F

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30 November 2017

Combes A

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30 November 2017

Towbin J

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30 November 2017

Craigen WJ

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30 November 2017

Gibbs R

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30 November 2017

publication date

1 October 2002

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30 November 2017

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30 November 2017

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30 November 2017

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30 November 2017

page(s)

298-304

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Noonan syndrome: the changing phenotype

30 November 2017

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

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7 January 2021

Noonan syndrome: a clinical and genetic study of 31 patients

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Terminal differentiation of chondrocytes in culture is a spontaneous process and is arrested by transforming growth factor-beta 2 and basic fibroblast growth factor in synergy

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Neurofibromatosis-Noonan syndrome

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7 January 2021

Noonan syndrome: partial factor XI deficiency

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7 January 2021

Noonan syndrome and aortic coarctation

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7 January 2021

King syndrome: further clinical variability and review of the literature

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7 January 2021

Cardiovascular abnormalities in Noonan syndrome: the clinical findings and treatments

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Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family

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7 January 2021

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7 January 2021

Identifiers

DOI

10.1002/HUMU.10129

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30 November 2017

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