Cancer Risk in Patients With Noonan Syndrome Carrying a PTPN11 Mutation

European Journal of Human Genetics - United Kingdom
doi 10.1038/ejhg.2011.37
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome

Case Reports in Neurological Medicine
2019English

Noonan Syndrome: Comparing Mutation-Positive With Mutation-Negative Dutch Patients

Molecular Syndromology
Genetics
2013English

Response to Growth Hormone Therapy in Children With Noonan Syndrome: Correlation With or Without PTPN11 Gene Mutation

Hormone Research in Paediatrics
Child HealthEndocrinologyPerinatologyPediatricsMetabolismDiabetes
2012English

Genotype and Phenotype in Patients With Noonan Syndrome and a RIT1 Mutation

Genetics in Medicine
MedicineGenetics
2016English

Congenital Chylothorax as the Initial Presentation of PTPN11-Associated Noonan Syndrome

Journal of Pediatrics
Child HealthPediatricsPerinatology
2017English

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

American Journal of Human Genetics
Genetics
2002English

PTPN11 Mutations in Patients With LEOPARD Syndrome: A French Multicentric Experience

Journal of Medical Genetics
Genetics
2004English

Heart Failure in a Patient With Noonan Syndrome

Circulation
Cardiovascular MedicinePhysiologyCardiology
2011English

Transient Myeloproliferative Disorder in an Infant With PTPN11 Mutation

British Journal of Haematology
Hematology
2017English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy