Associated Papers
Variants in ALX4 and their association with genitourinary defects.
Chen CH et al.
Andrology, 2020
Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2.
El-Ruby M et al.
American Journal of Medical Genetics. Part A, 2018
[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
Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.
Mavrogiannis LA et al.
Nature Genetics, 2001
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