|
| << previous | next >> |
Journal description
All volumes of the corresponding journal
All issues of the corresponding volume
All articles of the corresponding issues
Details for article 15 of 16 found articles
| Title: |
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype |
| Author: |
Motta, Marialetizia Fasano, Giulia Gredy, Sina Brinkmann, Julia Bonnard, Adeline Alice Simsek-Kiper, Pelin Ozlem Gulec, Elif Yilmaz Essaddam, Leila Utine, Gulen Eda Guarnetti Prandi, Ingrid Venditti, Martina Pantaleoni, Francesca Radio, Francesca Clementina Ciolfi, Andrea Petrini, Stefania Consoli, Federica Vignal, Cédric Hepbasli, Denis Ullrich, Melanie de Boer, Elke Vissers, Lisenka E.L.M. Gritli, Sami Rossi, Cesare De Luca, Alessandro Ben Becher, Saayda Gelb, Bruce D. Dallapiccola, Bruno Lauri, Antonella Chillemi, Giovanni Schuh, Kai Cavé, Hélène Zenker, Martin Tartaglia, Marco |
| Appeared in: |
The American journal of human genetics |
| Paging: | Volume 108 () nr. 11 pages 2112-2129 |
| Year: |
2021 |
| Contents: | |
| Publisher: |
American Society of Human Genetics |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 15 of 16 found articles
| << previous | next >> |