Associated Papers
The role of Rho GTPases in facial morphogenesis.
Ibrahim I et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists, 2026
Four putative pathogenic ARHGAP29 variants in patients with non-syndromic orofacial clefts (NsOFC).
Ranji P et al.
European Journal of Human Genetics : Ejhg, 2025
Functional Validation of Noncoding Variants Associated With Nonsyndromic Orofacial Cleft.
Zhu S et al.
Human Mutation, 2025
40918684 (PubMed )
Supplement: 6824122.f4.xlsx › Table_S4
A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate.
Yu Q et al.
The Journal of Maternal-fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2022
Identification of a Novel Variant of ARHGAP29 in a Chinese Family with Nonsyndromic Cleft Lip and Palate.
Tang JX et al.
Biomed Research International, 2020
Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants.
Savastano CP et al.
Clinical Genetics, 2017
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