European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe-Reference-Cited by-同舟云学术

European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe

Published:2022-01 Issue:1 Volume:65 Page:104371
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

García-Miñaúr Sixto,Burkitt-Wright Emma^ORCID,Verloes Alain,Shaikh Guftar^ORCID,Lebl Jan^ORCID,Östman-Smith Ingegerd,Wolf Cordula M.,Ortega Castelló Eduardo,Tartaglia Marco,Zenker Martin,Edouard Thomas^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference41 articles.

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2. The face of Noonan syndrome: does phenotype predict genotype;Allanson;Am. J. Med. Genet.,2010

3. Targeted ultrasound examination and DNA testing for Noonan syndrome, in fetuses with increased nuchal translucency and normal karyotype;Bakker;Prenat. Diagn.,2011

4. Prenatal features of Noonan syndrome: prevalence and prognostic value;Baldassarre;Prenat. Diagn.,2011

5. Constitutional bone impairment in Noonan syndrome;Baldassarre;Am. J. Med. Genet.,2017

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