Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Screening for MSX1 and PAX9 gene variants among hypodontia patients in the Jordanian population.

Cellular and molecular biology (Noisy-le-Grand, France) - 13 Feb 2026

Quran Areej, Maslat Ahmed, Jaradat Saied, Hammouri Eman, Quran Abeer

Abstract excerpt

This study aimed to sequence the PAX9 and MSX1 genes in a group of Jordanian patients diagnosed with non-syndromic hypodontia. The study also examined whether the identified genetic variants in these key odontogenic genes could be used to assess susceptibility to hypodontia. Fifty Jordanian individuals diagnosed with non-syndromic hypodontia were enrolled in this study. Genomic DNA was extracted, and all exons of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anodontia
Share to Exons
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Jordan

Share to MSX1 Transcription Factor

Share to PAX9 Transcription Factor

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 41684174
DOI: 10.14715/cmb/2025.72.1.6

Genes

MSX1
PAX9

Variants

rs36059701
rs567549350

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Screening for MSX1 and PAX9 gene variants among hypodontia patients in the Jordanian population.PMID 41684174Read ↗

Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.Semantic proximity Read ↗

Orodental malformations associated with human MSX1 sequence variants.Semantic proximity Read ↗

Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.Semantic proximity Read ↗

A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesis.Semantic proximity Read ↗

A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.Semantic proximity Read ↗

MSX1 gene polymorphisms in non-syndromic cleft lip and/or palate.Semantic proximity Read ↗

Sequence analysis of PAX9, MSX1 and AXIN2 genes in a Chinese oligodontia family.Semantic proximity Read ↗

Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia.Semantic proximity Read ↗

Family and case-control genetic study of MSX1 polymorphisms in peg-shaped teeth Jordanian population.Semantic proximity Read ↗

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

PAX9 polymorphisms and susceptibility with sporadic tooth agenesis in Turkish populations: a case-control study.Semantic proximity Read ↗

A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.