(Q34687343)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19220331%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

title

Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta (English)

1 reference

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21 January 2020

5

1 reference

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21 January 2020

Sangwoo T Han

6

1 reference

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21 January 2020

Erhan Firatli

8

1 reference

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21 January 2020

author name string

P S Hart

1

1 reference

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21 January 2020

S Becerik

2

1 reference

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21 January 2020

D Cogulu

3

1 reference

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21 January 2020

G Emingil

4

1 reference

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21 January 2020

P P Sulima

7

1 reference

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21 January 2020

T C Hart

9

1 reference

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21 January 2020

publication date

11 February 2009

1 reference

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21 January 2020

1 reference

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21 January 2020

volume

75

1 reference

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21 January 2020

issue

4

1 reference

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21 January 2020

page(s)

401-404

1 reference

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

21 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=4264522

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 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264522

FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264522

MMP20 active-site mutation in hypomaturation amelogenesis imperfecta

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264522

MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264522

Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264522

Relationship of phenotype and genotype in X-linked amelogenesis imperfecta

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264522

Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264522

The enamel proteins in human amelogenesis imperfecta.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264522

Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4264522

Changes in the protein components of rat incisor enamel during tooth development

7 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19220331

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1399-0004.2008.01112.X

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19220331%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19220331%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

PubMed publication ID

19220331

1 reference