(Q28211356)

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A nomenclature for X-linked amelogenesis imperfecta

scientific article (publication date: April 2002)

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Europe PubMed Central

title

A nomenclature for X-linked amelogenesis imperfecta (English)

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main subject

amelogenesis imperfecta

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P S Hart

1

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T C Hart

series ordinal

2

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J P Simmer

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3

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J T Wright

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4

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language of work or name

English

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publication date

April 2002

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published in

Archives of Oral Biology

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volume

47

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issue

4

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page(s)

255-60

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cites work

Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

An amelogenin gene defect associated with human X-linked amelogenesis imperfecta

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

Mutational analysis of X-linked amelogenesis imperfecta in multiple families

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

Detection of a novel mutation in X-linked amelogenesis imperfecta

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1)

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1)

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

Specific amelogenin gene splice products have signaling effects on cells in culture and in implants in vivo

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

Partial expression of sex-linked recessive amelogenesis imperfecta in females compatible with the Lyon hypothesis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0003-9969%2802%2900005-5

retrieved

7 January 2021

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Identifiers

DOI

10.1016/S0003-9969(02)00005-5

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PubMed publication ID

11922868

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(Q28211356)

A nomenclature for X-linked amelogenesis imperfecta

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