Rapid detection by hydrops panel of Noonan syndrome with PTPN11 mutation (p.Thr73Ile) and persistent thrombocytopenia-Reference-Cited by-同舟云学术

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

Author:

Schönfeld Mascha¹^ORCID,Selig Mareike²,Russo Alexandra³,Lindner Christine⁴,Kampmann Christoph⁵,Mildenberger Eva¹,Whybra Catharina¹^ORCID

Affiliation:

1. Neonatology University Medical Center of the Johannes Gutenberg University Mainz Germany

2. Institute of Human Genetics University Medical Center of the Johannes Gutenberg University Mainz Germany

3. Hematology University Medical Center of the Johannes Gutenberg University Mainz Germany

4. Department of Obstetrics and Gynecology University Medical Center of the Johannes Gutenberg University Mainz Germany

5. Pediatric Cardiology Department of Pediatrics University Medical Center of the Johannes Gutenberg University Mainz Germany

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

Reference22 articles.

Cited by 4 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