Results 161 to 170 of about 12,486 (245)
Ophthalmic phenotype associated with a novel mutation in <i>LAMB3</i> gene linked to uncommon Intermediate Junctional Epidermolysis Bullosa. [PDF]
Alzaben KA +5 more
europepmc +1 more source
PAX9 Mutation of Non-Syndromic Hypodontia in a Malaysian Family
Nur Farahiyah Mohamed Idrus +5 more
openalex +2 more sources
Full Mouth Rehabilitation of a Rare Case of Hypodontia: A Case Report. [PDF]
Aminianpour N, Zeighami S.
europepmc +1 more source
Dental Anomalies: Prevalence, Patterns of Association and Relationship With Dental Age. [PDF]
Loscertales-Martín-de-Agar B +4 more
europepmc +1 more source
Influences of genetic and environmental factors on developmental dental anomalies: a twin study. [PDF]
Budak I, Oz E.
europepmc +1 more source
Oral Manifestations in Adolescents with Genetic Syndromes: A Retrospective Cross-Sectional Study. [PDF]
Țenț A +5 more
europepmc +1 more source
Concomitant hypodontia and hyperdontia: A report of two cases
Nitesh Tewari +2 more
openalex +2 more sources

