(Q24643670)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

title

Phenotypic variation in FAM83H-associated amelogenesis imperfecta (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

main subject

amelogenesis imperfecta

1 reference

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

author name string

J T Wright

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

S Frazier-Bowers

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

D Simmons

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

K Alexander

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

P Crawford

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

P S Hart

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

T C Hart

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

language of work or name

English

0 references

publication date

1 April 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

Journal of Dental Research

27 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

volume

88

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

page(s)

356-360

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

Mutational spectrum of FAM83H: the C-terminal portion is required for tooth enamel calcification

27 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Competency for nonsense-mediated reduction in collagen X mRNA is specified by the 3' UTR and corresponds to the position of mutations in Schmid metaphyseal chondrodysplasia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

The molecular etiologies and associated phenotypes of amelogenesis imperfecta

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Enamelin and autosomal-dominant amelogenesis imperfecta.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Relationship of phenotype and genotype in X-linked amelogenesis imperfecta

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Segregation analysis of mandibular prognathism in Libya

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Amelogenesis imperfecta: prevalence and incidence in a northern Swedish county

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Amelogenesis imperfecta among Israeli Jews and the description of a new type of local hypoplastic autosomal recessive amelogenesis imperfecta

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Craniofacial features associated with amelogenesis imperfecta

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Prevalence of malocclusion and orthodontic treatment need in the United States: estimates from the NHANES III survey

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

The enamel proteins in human amelogenesis imperfecta.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Hereditary amelogenesis imperfecta. An epidemiological, genetic and clinical study in a Swedish child population

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Variation in dental and skeletal open bite malocclusion in humans with amelogenesis imperfecta.

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1177%2F0022034509333822

Relationship of Phenotype and Genotype in X-Linked Amelogenesis Imperfecta

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1177%2F0022034509333822

The mineral and protein content of enamel in amelogenesis imperfecta

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2754853

Major gene and multifactorial inheritance of mandibular prognathism

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19407157

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hereditary defects in enamel and dentin

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19407157

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Human enamel phenotype associated with amelogenesis imperfecta and a kallikrein-4 (g.2142G>A) proteinase mutation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19407157

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1177/0022034509333822

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19407157%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

1 reference