(Q77889904)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

title

Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

main subject

amelogenesis imperfecta

1 reference

M J Aldred

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

R Savarirayan

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

S R Lamandé

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

P J M Crawford

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

publication date

1 January 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

page(s)

62-68

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

Amelogenesis imperfecta: a genetic study

9 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

Amelogenesis imperfecta with taurodontism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

Tricho-dento-osseous syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

Genetic linkage of the tricho-dento-osseous syndrome to chromosome 17q21

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

Dental abnormalities in the tricho-dento-osseous syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

Tricho-dento-osseous syndrome: a scanning electron microscopic analysis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

Clinical heterogeneity in the tricho-dento-osseous syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.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.1601-0825.2002.1C766.X

7 January 2021

Tricho-dento-osseous syndrome: heterogeneity or clinical variability

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

Tricho-dento-osseous syndrome. Features of the hair and teeth

1 reference

https://api.crossref.org/works/10.1034%2FJ.1601-0825.2002.1C766.X

7 January 2021

10.1034/J.1601-0825.2002.1C766.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11936459%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference