Associated Papers
Decoding the mechanisms of cooperative DNA binding by the Paired-like homeodomain family.
Cain B et al.
Biorxiv : the Preprint Server for Biology, 2025
41279221 (PubMed )
Supplement: media-2.xlsx › SuppTable2
The ALX4 dimer structure provides insight into how disease alleles impact function.
Cain B et al.
Nature Communications, 2025
Clinical interest of molecular study in cases of isolated midline craniosynostosis.
Di Rocco F et al.
European Journal of Human Genetics : Ejhg, 2023
Variants in ALX4 and their association with genitourinary defects.
Chen CH et al.
Andrology, 2020
A Novel Missense Variant in the ALX4 Gene Underlies Mild to Severe Frontonasal Dysplasia in a Consanguineous Family.
Hussain S et al.
Genetic Testing and Molecular Biomarkers, 2020
Mild nasal clefting may be predictive for ALX4 heterozygotes.
Altunoglu U et al.
American Journal of Medical Genetics. Part A, 2014
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