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Foramina parietalia permagna: Clinical radiological evaluation of a Spanish family with an undescribed mutation in the ALX4 gene.

Anales de pediatria - 1 Aug 2021

Bote Gascón Marta, Martínez Del Río Carmen, García Ron Adrián

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PMID: 34315693
DOI: 10.1016/j.anpede.2020.07.018

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Related research

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Research trail→

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Foramina parietalia permagna: Clinical radiological evaluation of a Spanish family with an undescribed mutation in the ALX4 gene.PMID 34315693Read ↗

A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP).Semantic proximity Read ↗

The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).Semantic proximity Read ↗

A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly.Semantic proximity Read ↗

Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutation.Semantic proximity Read ↗

Mild nasal clefting may be predictive for ALX4 heterozygotes.Semantic proximity Read ↗

Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2Semantic proximity Read ↗

Syndromic foramina parietalia permagna.Semantic proximity Read ↗

Foramina parietalia permagna: the ins and outs.Semantic proximity Read ↗

Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.Semantic proximity Read ↗

Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutations.Semantic proximity Read ↗

Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.Semantic proximity Read ↗

A case of tibial hemimelia in a German Galloway calf is associated with a novel mutation in the ALX4 gene.Semantic proximity Read ↗

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