(Q52126512)

22 April 2018

review article

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title

Dentinogenesis imperfecta-associated syndromes. (English)

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22 April 2018

author name string

Kantaputra PN

series ordinal

1

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22 April 2018

publication date

1 November 2001

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22 April 2018

American Journal of Medical Genetics Part A

published in

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22 April 2018

volume

104

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22 April 2018

page(s)

75-78

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22 April 2018

issue

1

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22 April 2018

Type II collagen defect in two sibs with the Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxity

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Dentine is biochemically abnormal in osteogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Scanning electron microscopy of teeth in dominant osteogenesis imperfecta: support for genetic heterogeneity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Scanning electron microscopy of teeth in osteogenesis imperfecta type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Evaluation of oral problems in an osteogenesis imperfecta population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Novel COL1A1 mutation (G559C) [correction of G599C] associated with mild osteogenesis imperfecta and dentinogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

The non-collagenous dentin matrix proteins are involved in dentinogenesis imperfecta type II (DGI-II).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

DSPP mutation in dentinogenesis imperfecta Shields type II

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Refinement of the dentinogenesis imperfecta type II locus to an interval of less than 2 centiMorgans at chromosome 4q21 and the creation of a yeast artificial chromosome contig of the critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Familial dentinogenesis imperfecta, blue sclerae, and wormian bones without fractures: another type of osteogenesis imperfecta?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Dental findings in the Schimke immuno-osseous dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Unique dwarfing, spondylometaphyseal skeletal dysplasia, with joint laxity and dentinogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

A Polish variant of isolated dentinogenesis imperfecta with a generalised connective tissue defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Discrimination of morphological findings in dentine from osteogenesis imperfecta patients using combinations of polarized light microscopy, microradiography and scanning electron microscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Refined mapping of the human dentin sialophosphoprotein (DSPP) gene within the critical dentinogenesis imperfecta type II and dentin dysplasia type II loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Heterogeneity of osteogenesis imperfecta type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Reduced expression of dentin sialophosphoprotein is associated with dysplastic dentin in mice overexpressing transforming growth factor-beta 1 in teeth

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Hyperfibers and vesicles in dentin matrix in dentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

Phenotypical features of an unique Irish family with severe autosomal recessive osteogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10031

21 January 2018

Identifiers

DOI

10.1002/AJMG.10031

1 reference

22 April 2018

PubMed ID

11746032

1 reference

22 April 2018