Comment on “Prenatal diagnosis and prognosis in Noonan syndrome”
Author:
Affiliation:
1. Department of Pediatrics; University of Torino; Torino Italy
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.4234/fullpdf
Reference13 articles.
1. Postnatal phenotype according to prenatal ultrasound features of Noonan syndrome a retrospective study of 28 cases;Gaudineau;Prenat Diagn,2013
2. Noonan syndrome and clinically related disorders;Tartaglia;Best Pract Res Clin Endocrinol Metab,2011
3. Transcriptional hallmarks of Noonan syndrome and Noonan-like syndrome with loose anagen hair;Ferrero;Hum Mutat,2012
4. The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation;Tidyman;Curr Opin Genet Dev,2009
5. SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations;Lepri;Hum Mutat,2011
Cited by 3 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. Genetic Evaluation of Fetal Sonographic Abnormalities;Perinatal Genetics;2019
2. Constitutional bone impairment in Noonan syndrome;American Journal of Medical Genetics Part A;2017-02-17
3. Phenotypic variability associated with the invariantSHOC2c.4A>G (p.Ser2Gly) missense mutation;American Journal of Medical Genetics Part A;2014-10-20
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