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Article

Novel homozygous ALX4 mutation causing frontonasal dysplasia-2 in a patient with meningoencephalocele.

Clinical genetics - 1 Dec 2015

Meloni V A, Moysés-Oliveira M, Melo M C C, Caneloi T P, Dantas A G, Soares M F F, Fock R, Rodrigues de Nicola P D, Dias-da-Silva M R, Melaragno M I

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25963140
DOI: 10.1111/cge.12595

Genes

ALX4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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Novel homozygous ALX4 mutation causing frontonasal dysplasia-2 in a patient with meningoencephalocele.PMID 25963140Read ↗

Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2.Semantic proximity Read ↗

Vertical transmission of a frontonasal phenotype caused by a novel ALX4 mutation.Semantic proximity Read ↗

A Novel Missense Variant in the ALX4 Gene Underlies Mild to Severe Frontonasal Dysplasia in a Consanguineous Family.Semantic proximity Read ↗

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

Potocki-Shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype.Semantic proximity Read ↗

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

Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia.Semantic proximity Read ↗

<i>ALX1</i> -related Frontonasal Dysplasia Results From Defective Neural Crest Cell Development and MigrationSemantic proximity Read ↗

Sneddon syndrome associated with two novel ADA2 gene mutations.Semantic proximity Read ↗

Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies.Semantic proximity Read ↗

Additional EFNB1 mutations in craniofrontonasal syndrome.Semantic proximity Read ↗

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