(Q33872472)

29 July 2017

title

Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions (English)

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29 July 2017

main subject

amelogenesis imperfecta

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Price JA

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29 July 2017

Wright JT

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29 July 2017

Walker SJ

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29 July 2017

Crawford PJ

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29 July 2017

Aldred MJ

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29 July 2017

Hart TC

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29 July 2017

publication date

1 July 1999

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29 July 2017

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29 July 2017

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29 July 2017

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29 July 2017

page(s)

35-40

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Identification of a mutation in DLX3 associated with tricho-dento- osseous (TDO) syndrome

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

Dlx and other homeobox genes in the morphological development of the dentition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

Genomic analysis of a new mammalian distal-less gene: Dlx7

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

Differential and overlapping expression domains of Dlx-2 and Dlx-3 suggest distinct roles for Distal-less homeobox genes in craniofacial development

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

Enamel structure and composition in the tricho-dento-osseous syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: separate conditions or a spectrum of disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

7 January 2021

Taurodontism of the mandibular first permanent molar distinguishes between the tricho-dento-osseous (TDO) syndrome and amelogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

7 January 2021

Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

7 January 2021

Identification of a CA/TG repeat polymorphism proximal to the human DLX3 gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550105.X

7 January 2021

10.1034/J.1399-0004.1999.550105.X

Identifiers

DOI

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29 July 2017

1 reference