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

Parent-of-origin effects for MSX1 in a Chilean population with nonsyndromic cleft lip/palate.

American journal of medical genetics. Part A - 1 Aug 2010

Suazo José, Santos José Luis, Jara Lilian, Blanco Rafael

Abstract excerpt

Based on association and sequencing studies, investigators have postulated muscle segment homeobox 1 (MSX1) as a strong candidate gene involved in the causation of nonsyndromic cleft lip with or without cleft palate (NSCLP). Parent-of-origin effects have been suggested for some NSCLP candidate genes but not for MSX1. The aims of the present study were to test for allele/haplotype associations applying the...

Read the complete abstract on PubMed

Topics

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

Share to Chile
Share to Cleft Lip
Share to Cleft Palate

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Markers

Share to Genomic Imprinting

Share to Linkage Disequilibrium

Share to MSX1 Transcription Factor

Share to Parents

Source

Identifiers

PMID: 20635363
DOI: 10.1002/ajmg.a.33528

Genes

MSX1
TAT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Parent-of-origin effects for MSX1 in a Chilean population with nonsyndromic cleft lip/palate.PMID 20635363Read ↗

Association between MSX1 SNPs and nonsyndromic cleft lip with or without cleft palate in the Korean population.Semantic proximity Read ↗

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

MSX1 gene polymorphisms in Mexican patients with non-syndromic cleft lip/palate.Semantic proximity Read ↗

Association of MSX1 c.*6C > T Variant with Nonsyndromic Cleft Lip With or Without Cleft Palate in Turkish Patients.Semantic proximity Read ↗

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

MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.Semantic proximity Read ↗

Association of MSX1 799 G>T variant with nonsyndromic cleft lip/palate in South Indian adolescent patients.Semantic proximity Read ↗

Role of MSX1 in the development of non-syndromic clefts in the sub-Himalayan region of India.Semantic proximity Read ↗

Investigation of Parental Transmission of RUNX2 Single Nucleotide Polymorphism and Its Association With Nonsyndromic Cleft Lip With or Without Palate.Semantic proximity Read ↗

Gene-gene interaction for nonsyndromic cleft lip with or without cleft palate in Chilean case-parent trios.Semantic proximity Read ↗

Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations.Semantic proximity Read ↗

MSX1 polymorphism associated with risk of oral cleft in Korea: evidence from case-parent trio and case-control studies.Semantic proximity Read ↗

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