Associated Papers
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
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients.
Roscioli T et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2013
The natural history of patients treated for TWIST1-confirmed Saethre-Chotzen syndrome.
Foo R et al.
Plastic and Reconstructive Surgery, 2009
Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations.
Seto ML et al.
American Journal of Medical Genetics. Part A, 2007
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