Noonan Syndrome: Clinical Aspects and Molecular Pathogenesis
Author:
Publisher
S. Karger AG
Subject
Genetics (clinical),Genetics
Cited by 185 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Further characteristics of Noonan Syndrome type 13 caused by MAPK1 loss of function variant: Case report and literature review;Medicine: Case Reports and Study Protocols;2024-09
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3. Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant;European Journal of Human Genetics;2024-06-01
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