← Evidence map

ArticleMolecular genetics & genomic medicine2020

Rapid detection by hydrops panel of Noonan syndrome with PTPN11 mutation (p.Thr73Ile) and persistent thrombocytopenia.

Mascha Schönfeld et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

4 papers cite it

2020
2021
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 32144894