(Q36929652)

17 August 2017

Identification of microdeletions in candidate genes for cleft lip and/or palate (English)

1 reference

17 August 2017

1 reference

Allen J Wilcox

8

0 references

Kaare Christensen

object named as

Kaare Christensen

6

0 references

Adrianna Mostowska

2

object named as

Adrianna Mostowska

1 reference

17 August 2017

Min Shi

1

1 reference

17 August 2017

Astanand Jugessur

3

1 reference

17 August 2017

Marla K Johnson

4

1 reference

17 August 2017

Maria Adela Mansilla

5

1 reference

17 August 2017

Rolv T Lie

7

1 reference

17 August 2017

Jeffrey C Murray

9

1 reference

17 August 2017

language of work or name

1 reference

1 January 2009

1 reference

Birth Defects Research Part A: Clinical and Molecular Teratology

17 August 2017

1 reference

17 August 2017

85

1 reference

17 August 2017

1

1 reference

17 August 2017

42-51

1 reference

Mapping and sequencing of structural variation from eight human genomes

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

TFAP2A mutations result in branchio-oculo-facial syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

FGF signalling and SUMO modification: new players in the aetiology of cleft lip and/or palate

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Impaired FGF signaling contributes to cleft lip and palate

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Folic acid supplements and risk of facial clefts: national population based case-control study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

SUMO1 haploinsufficiency leads to cleft lip and palate

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Orofacial clefting: recent insights into a complex trait

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Changing lifestyles and oral clefts occurrence in Denmark

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

mBtd is required to maintain signaling during murine limb development

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Sp8 is crucial for limb outgrowth and neuropore closure

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

T-box genes in human disorders

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Gene/environment causes of cleft lip and/or palate

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Transcription factor AP-2 essential for cranial closure and craniofacial development

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Maternal smoking and oral clefts: the role of detoxification pathway genes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Common deletion polymorphisms in the human genome.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

Prevalence of duplications and deletions of the 22q11 DiGeorge syndrome region in a population-based sample of infants with cleft palate

4 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FBDRA.20571

Parent's Occupation and Isolated Orofacial Clefts in Norway: A Population-based Case-control Study

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3682790

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

4 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19137569

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A high-resolution survey of deletion polymorphism in the human genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19137569

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/BDRA.20571

1 reference

17 August 2017

1 reference

17 August 2017

1 reference