Results 131 to 140 of about 3,948 (205)

Rare Findings in Cleidocranial Dysplasia Caused by RUNX Mutation. [PDF]

Glob Med Genet, 2022
Kalayci Yigin A, Duz MB, Seven M.
europepmc   +1 more source

Cleidocranial dysplasia and novel RUNX2 variants: dental, craniofacial, and osseous manifestations. [PDF]

J Appl Oral Sci, 2022
Thaweesapphithak S, Saengsin J, Kamolvisit W, Theerapanon T, Porntaveetus T, Shotelersuk V.   +5 more
europepmc   +1 more source

Disturbances of Dental Development in Cleidocranial Dysplasia. [PDF]

J Craniofac Surg
The VR, Dhamo B, Wolvius EB.
europepmc   +1 more source

Radiographic features of cleidocranial dysplasia on panoramic radiographs. [PDF]

Imaging Sci Dent, 2021
Symkhampha K, Ahn GS, Huh KH, Heo MS, Lee SS, Kim JE.   +5 more
europepmc   +1 more source

Clinical and Radiological Spectrum in Cleidocranial Dysplasia: A Case Series. [PDF]

Curr Health Sci J
Debta FM, Agarwal K, Bera B, Panda R, Murmu S.   +4 more
europepmc   +1 more source

A Chinese premature infant with cleidocranial dysplasia characterized by heterozygous RUNX2 mutation and cerebral infarction: a case report. [PDF]

Front Pediatr
Zhao W, An Y, Zhang X, Zhuo N, Cai C, Arigong G.   +5 more
europepmc   +1 more source

An Exploration of Mutagenesis in a Family with Cleidocranial Dysplasia without RUNX2 Mutation. [PDF]

Front Genet, 2021
Liu D, Liu Y, Zhang X, Wang Y, Zhang C, Zheng S.   +5 more
europepmc   +1 more source

Cleidocranial Dysplasia With Multiple Impacted Teeth and Dentigerous Cysts: A Case Report of a Rare Entity. [PDF]

Cureus
Shinh M.
europepmc   +1 more source

Inhibition of miR338 rescues cleidocranial dysplasia in Runx2 mutant mice partially via the Hif1a-Vegfa axis. [PDF]

Exp Mol Med, 2023
Jin R, Zhang H, Lin C, Guo J, Zou W, Chen Z, Liu H.   +6 more
europepmc   +1 more source

Dental aspects of systemic genetic diseases - Williams-Beuren syndrome and cleidocranial dysplasia [PDF]

, 2007
Balaton Gergely
core