(Q36457216)

14 August 2017

MSX1 and orofacial clefting with and without tooth agenesis (English)

1 reference

14 August 2017

A Modesto

1

1 reference

14 August 2017

L M Moreno

2

1 reference

14 August 2017

K Krahn

3

1 reference

14 August 2017

S King

4

1 reference

14 August 2017

A C Lidral

5

1 reference

14 August 2017

language of work or name

English

0 references

publication date

1 June 2006

1 reference

Journal of Dental Research

14 August 2017

1 reference

14 August 2017

85

1 reference

14 August 2017

6

1 reference

14 August 2017

542-546

1 reference

In a Vietnamese population, MSX1 variants contribute to cleft lip and palate

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

MSX1 and TGFB3 contribute to clefting in South America

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Multiplex relative risk and estimation of the number of loci underlying an inherited disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

The role of MSX1 in human tooth agenesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

A nonsense mutation in MSX1 causes Witkop syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Haploinsufficiency of MSX1: a mechanism for selective tooth agenesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Genetics of nonsyndromic oral clefts revisited

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

A review of tooth formation in children with cleft lip/palate

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Incidence of cleft lip, cleft palate, and cleft lip and palate among races: a review

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Hox-7, a mouse homeobox gene with a novel pattern of expression during embryogenesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Congenital absence of teeth: a review with emphasis on inheritance patterns

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

MSX1, PAX9, and TGFA contribute to tooth agenesis in humans.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Family-based analysis of MSX1 haplotypes for association with oral clefts.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

Variants of developmental genes (TGFA, TGFB3, and MSX1) and their associations with orofacial clefts: a case-parent triad analysis.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

A case-control study of nonsyndromic oral clefts in Maryland

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2241923

MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia

21 September 2018

1 reference

12 December 2020

Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families

1 reference

12 December 2020

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

1 reference

12 December 2020

A novelMSX1 mutation in hypodontia

1 reference

12 December 2020

Congenitally missing second premolars in cleft lip and cleft palate children

1 reference

12 December 2020

10.1177/154405910608500612

Identifiers

DOI

1 reference

14 August 2017

1 reference

14 August 2017

1 reference