(Q51848004)

14 April 2018

title

Dental developmental disturbances in 50 individuals with the 22q11.2 deletion syndrome; relation to medical conditions? (English)

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4

Ivar Følling

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6

Tore G Abrahamsen

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author name string

Hilde Nordgarden

1

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Kari Lima

2

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Nina Skogedal

3

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Kari Storhaug

5

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publication date

10 November 2011

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Acta Odontologica Scandinavica

published in

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volume

70

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issue

3

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page(s)

194-201

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Defining the clinical spectrum of deletion 22q11.2

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1 reference

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21 January 2018

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Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

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Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome

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Oral findings in DiGeorge syndrome: clinical features and histologic study of primary teeth.

21 January 2018

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Morphological appearance and chemical composition of enamel in primary teeth from patients with 22q11 deletion syndrome

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A regulatory relationship between Tbx1 and FGF signaling during tooth morphogenesis and ameloblast lineage determination.

21 January 2018

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Enamel-free teeth: Tbx1 deletion affects amelogenesis in rodent incisors

21 January 2018

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Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome

21 January 2018

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Tooth abnormalities and soft tissue changes in patients with velocardiofacial syndrome

21 January 2018

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Developmental defects of enamel in a group of New Zealand children: their prevalence and some associated etiological factors.

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The prevalence of demarcated opacities in permanent first molars in a group of Swedish children.

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Prevalence and Diagnosis of Molar-Incisor- Hypomineralisation (MIH): A systematic review

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Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.

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Clinical and microstructural aberrations of enamel of deciduous and permanent teeth in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.

21 January 2018

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21 January 2018

Identifiers

DOI

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14 April 2018

PubMed ID

22070626

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14 April 2018