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Journal description
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Details for article 15 of 52 found articles
| Title: |
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway |
| Author: |
Asif, Maria Kaygusuz, Emrah Shinawi, Marwan Nickelsen, Anna Hsieh, Tzung-Chien Wagle, Prerana Budde, Birgit S. Hochscherf, Jennifer Abdullah, Uzma Höning, Stefan Nienberg, Christian Lindenblatt, Dirk Noegel, Angelika A. Altmüller, Janine Thiele, Holger Motameny, Susanne Fleischer, Nicole Segal, Idan Pais, Lynn Tinschert, Sigrid Samra, Nadra Nasser Savatt, Juliann M. Rudy, Natasha L. De Luca, Chiara Paola Fortugno, White, Susan M. Krawitz, Peter Hurst, Anna C.E. Niefind, Karsten Jose, Joachim Brancati, Francesco Nürnberg, Peter Hussain, Muhammad Sajid |
| Appeared in: |
Human genetics and genomics advances |
| Paging: | Volume 3 () nr. 3 pages p. |
| Year: |
2022 |
| Contents: | |
| Publisher: |
The Authors |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 15 of 52 found articles
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