Associated Papers
Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance.
Tooze RS et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2023
Recurrent agnathia-otocephaly caused by DNA replication slippage in PRRX1.
Dasouki M et al.
American Journal of Medical Genetics. Part A, 2013
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