Results 241 to 250 of about 12,368 (291)

<i>Nkx2-3</i> Homeobox Gene Plays an Essential Role in Later Stages of Orofacial Differentiation. [PDF]

Ann Pediatr Child Health
Ruspita I, Das P, Kelangi S, Harvey RP, Bei M.   +4 more
europepmc   +1 more source

European Academy of Paeditric Dentistry: a guideline framework for undergraduate education in paediatric dentistry [PDF]

, 2009
Lygidakis, Nick, Marks, Luc, Veerkamp, Jaap, Welbury, Richard   +3 more
core   +1 more source

Acute Angle Closure Glaucoma in a Patient With Jalili-Smith Syndrome. [PDF]

Cureus
Suresh S, Zuberi HZ, Khandekar R, Buchanan EB, Kooner KS.   +4 more
europepmc   +1 more source

Navigating Complexity: A Case Report on a Comprehensive Dental Management Approach to Amelogenesis Imperfecta and Gingival Fibromatosis Syndrome. [PDF]

Cureus
Nasrallah H, Berro K.
europepmc   +1 more source

Long-term Survival Rate and Clinical Quality of Individually Layered Indirect Composite Restorations in Adolescents and Young Adults. [PDF]

J Adhes Dent
Hahn B, Holst AK, Ilse A, Haubitz I, Halbleib K, Krämer N, Krastl G, Soliman S.   +7 more
europepmc   +1 more source

Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability. [PDF]

J Med Genet
Smith CEL, Laugel-Haushalter V, Hany U, Best S, Taylor RL, Poulter JA, Wortmann SB, Feichtinger RG, Mayr JA, Al Bahlani S, Nikolopoulos G, Rigby A, Black GC, Watson CM, Mansour S, Inglehearn CF, Mighell AJ, Bloch-Zupan A, UK Inherited Retinal Disease Consortium, Genomics England Research Consortium.   +19 more
europepmc   +1 more source

Orofacial Anomalies in Kindler Epidermolysis Bullosa.

JAMA Dermatol
Krämer S, Hillebrecht AL, Wang Y, Badea MA, Barrios JI, Danescu S, Fuentes I, Kartal D, Klausegger A, Ponce de León E, Schilke R, Yordanova I, Bloch-Zupan A, Has C.   +13 more
europepmc   +1 more source

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Molecular-based phenotype variations in amelogenesis imperfecta.

Oral Diseases, 2023
Amelogenesis imperfecta (AI) is one of the typical dental genetic diseases in human. It can occur isolatedly or as part of a syndrome. Previous reports have mainly clarified the types and mechanisms of nonsyndromic AI.
Jing Dong, Wenyan Ruan, X. Duan
semanticscholar   +1 more source