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Article

Polymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders.

Clinical genetics - 1 Aug 1998

Hollway G E, Mulley J C

Abstract excerpt

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Topics

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Share to Chromosomes, Human, Pair 4
Share to Genes, Homeobox
Share to Growth Disorders
Share to Heteroduplex Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homeodomain Proteins

Share to Introns

Share to MSX1 Transcription Factor

Share to Polymorphism, Single-Stranded Conformational

Source

Identifiers

PMID: 9761395
DOI: 10.1111/j.1399-0004.1998.tb03719.x

Genes

MSX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Polymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders.PMID 9761395Read ↗

Studying ultra-rare variants in STX1A uncovers a novel neurodevelopmental disorder.Semantic proximity Read ↗

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.Semantic proximity Read ↗

Homeobox genes and human genetic disorders.Semantic proximity Read ↗

MSH homeobox 1 polymorphisms and the risk of non-syndromic orofacial clefts: a meta-analysis.Semantic proximity Read ↗

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.Semantic proximity Read ↗

Mutations in the human homeobox MSX1 gene in the congenital lack of permanent teeth.Semantic proximity Read ↗

Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous familySemantic proximity Read ↗

Deleterious coding variants in multi-case families with non-syndromic cleft lip and/or palate phenotypes.Semantic proximity Read ↗

MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.Semantic proximity Read ↗

MSX1 gene and nonsyndromic oral clefts in a Southern Brazilian population.Semantic proximity Read ↗

MSX1 and orofacial clefting with and without tooth agenesis.Semantic proximity Read ↗

Novel MSX1 variants identified in families with nonsyndromic oligodontiaSemantic proximity Read ↗

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