학술논문
Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance
Document Type
Article
Author
Tooze, R.S.; Miller, K.A.; Calpena, E.; Phipps, J.M.; Twigg, S.R.F.; Wilkie, A.O.M.; Swagemakers, S.M.A.; McGowan, S.J.; Boute, O.; Vanlerberghe, C.; Collet, C.; Johnson, D.; Wall, S.A.; Laffargue, F.; de Leeuw, N.; Ockeloen, C.W.; Morton, J.V.; Noons, P.; Tan, T.Y.; Timberlake, A.T.; Weber, A.; Wilson, L.C.; Zackai, E.H.; Mathijssen, I.M.J.
Source
In: Genetics in Medicine . (Genetics in Medicine, September 2023, 25(9))
Subject
Language
English
ISSN
15300366
10983600
10983600