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Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation

Crossref DOI link: https://doi.org/10.1038/gim.2016.32

Published Print: 2016-12

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Kouz, Karim

Lissewski, Christina https://orcid.org/0000-0002-5414-7126
Spranger, Stephanie

Mitter, Diana

Riess, Angelika

Lopez-Gonzalez, Vanesa

Lüttgen, Sabine

Aydin, Hatip https://orcid.org/0000-0003-4488-3186
von Deimling, Florian

Evers, Christina

Hahn, Andreas https://orcid.org/0000-0003-0235-5211
Hempel, Maja

Issa, Ulrike

Kahlert, Anne-Karin https://orcid.org/0000-0002-3201-2642
Lieb, Adrian

Villavicencio-Lorini, Pablo

Ballesta-Martinez, Maria Juliana

Nampoothiri, Sheela

Ovens-Raeder, Angela

Puchmajerová, Alena

Satanovskij, Robin

Seidel, Heide

Unkelbach, Stephan

Zabel, Bernhard https://orcid.org/0000-0002-7796-2991
Kutsche, Kerstin

Zenker, Martin
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Text and Data Mining valid from 2016-12-01

Text and Data Mining valid from 2016-12-01

Version of Record valid from 2022-01-19
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This article is maintained by: Elsevier

Article Title: Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2016.32

Content Type: article

Copyright: © 2016, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics