Results 141 to 150 of about 15,266 (165)

AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta. [PDF]

Int J Mol Sci
Wang SK, Zhang H, Lin HC, Wang YL, Lin SC, Seymen F, Koruyucu M, Simmer JP, Hu JC.   +8 more
europepmc   +1 more source

[Frameshift mutation in RELT gene causes amelogenesis imperfecta]. [PDF]

Beijing Da Xue Xue Bao Yi Xue Ban
Zhang Z, Xu X, Gao X, Dong Y, Tian H.
europepmc   +1 more source

IP3 receptor depletion in a spontaneous canine model of Charcot-Marie-Tooth disease 1J with amelogenesis imperfecta. [PDF]

PLoS Genet
Hytönen MK, Rönkkö J, Hundi S, Jokinen TS, Suonto E, Teräväinen E, Donner J, La Rovere R, Bultynck G, Ylikallio E, Tyynismaa H, Lohi H.   +11 more
europepmc   +1 more source

Amelogénesis imperfecta en una familia

Revista Cubana de Estomatología
Paula Hurtado-Villa, Fabián Tobar-Tosse, Julio Osorio, Freddy Moreno   +3 more
doaj  

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Osteogenesis imperfecta

Nature Reviews Disease Primers, 2017
Nicholas Bishop, Peter H. Byers, Deborah Krakow   +2 more
exaly   +2 more sources

Dentinogenesis Imperfecta and Caries in Osteogenesis Imperfecta among Vietnamese Children

Dentistry Journal, 2021
Van Khanh Tran, Dung Chi Vu, Huong Thi Thu Nguyen   +2 more
exaly  

New perspectives on osteogenesis imperfecta

Nature Reviews Endocrinology, 2011
Aileen M Barnes, Wayne A Cabral, Joan C Marini   +2 more
exaly  

Osteogenesis imperfecta

Best Practice and Research in Clinical Rheumatology, 2008
Francis H Glorieux
exaly