(Q33903341)

29 July 2017

title

A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients (English)

1 reference

29 July 2017

Bernice E Morrow

9

0 references

Marcella Devoto

object named as

Marcella Devoto

10

0 references

Donna M McDonald-McGinn

4

object named as

Donna M McDonald-McGinn

1 reference

29 July 2017

author name string

Josine C C Widdershoven

1

1 reference

29 July 2017

Mark Bowser

2

1 reference

29 July 2017

Molly B Sheridan

3

1 reference

29 July 2017

Elaine H Zackai

5

1 reference

29 July 2017

Cynthia B Solot

6

1 reference

29 July 2017

Richard E Kirschner

7

1 reference

29 July 2017

Frits A Beemer

8

1 reference

29 July 2017

Beverly S Emanuel

11

1 reference

29 July 2017

publication date

31 October 2012

1 reference

International Journal of Pediatric Otorhinolaryngology

29 July 2017

published in

1 reference

29 July 2017

volume

77

1 reference

29 July 2017

issue

1

1 reference

29 July 2017

page(s)

123-127

1 reference

TGF-beta mediated FGF10 signaling in cranial neural crest cells controls development of myogenic progenitor cells through tissue-tissue interactions during tongue morphogenesis

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

PLINK: a tool set for whole-genome association and population-based linkage analyses

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Impaired FGF signaling contributes to cleft lip and palate

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

SUMO1 haploinsufficiency leads to cleft lip and palate

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Association between the transforming growth factor alpha gene and nonsyndromic oral clefts: a HuGE review

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Haploview: analysis and visualization of LD and haplotype maps

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Identification of SATB2 as the cleft palate gene on 2q32-q33.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

About face: signals and genes controlling jaw patterning and identity in vertebrates

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

FGF10 maintains stem cell compartment in developing mouse incisors

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

The Philadelphia story: the 22q11.2 deletion: report on 250 patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

The annual incidence of DiGeorge/velocardiofacial syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Periconceptional folate intake by supplement and food reduces the risk of nonsyndromic cleft lip with or without cleft palate

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098838

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23121717

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.IJPORL.2012.10.009

1 reference

29 July 2017

1 reference

29 July 2017

1 reference