Associated Papers
An additional whole-exome sequencing study in 102 panel-undiagnosed patients: A retrospective study in a Chinese craniosynostosis cohort.
Chen J et al.
Frontiers in Genetics, 2022
36118902 (PubMed )
Supplement: DataSheet1.XLSX › TableS2
An ENU-induced mutation in Twist1 transactivation domain causes hindlimb polydactyly with complete penetrance and dominant-negatively impairs E2A-dependent transcription.
Chen RZ et al.
Scientific Reports, 2020
32051525 (PubMed )
Supplement: 41598_2020_59455_MOESM3_ESM.pdf
Identification and analysis of the genetic causes in nine unrelated probands with syndromic craniosynostosis.
Xu Y et al.
Gene, 2018
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