Associated Papers
Clinical interest of molecular study in cases of isolated midline craniosynostosis.
Di Rocco F et al.
European Journal of Human Genetics : Ejhg, 2023
[Mother and son with enlarged parietal foramina, persistent fetal vein, and ALX4 mutation].
Morita M et al.
No to Hattatsu = Brain and Development, 2016
Skull defects, alopecia, hypertelorism, and notched alae nasi caused by homozygous ALX4 gene mutation.
Kariminejad A et al.
American Journal of Medical Genetics. Part A, 2014
Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.
Mavrogiannis LA et al.
European Journal of Human Genetics : Ejhg, 2006
Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplication.
Gentile M et al.
American Journal of Medical Genetics. Part A, 2004
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