Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance
- Resource Type
- Article
- Authors
- Tooze, Rebecca S.; Miller, Kerry A.; Swagemakers, Sigrid M.A.; Calpena, Eduardo; McGowan, Simon J.; Boute, Odile; Collet, Corinne; Johnson, David; Laffargue, Fanny; de Leeuw, Nicole; Morton, Jenny V.; Noons, Peter; Ockeloen, Charlotte W.; Phipps, Julie M.; Tan, Tiong Yang; Timberlake, Andrew T.; Vanlerberghe, Clemence; Wall, Steven A.; Weber, Astrid; Wilson, Louise C.; Zackai, Elaine H.; Mathijssen, Irene M.J.; Twigg, Stephen R.F.; Wilkie, Andrew O.M.
- Source
- In Genetics in Medicine September 2023 25(9)
- Subject
- Language
- ISSN
- 1098-3600