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]

open access: yesAm J Ophthalmol Case Rep
Alzaben KA   +5 more
europepmc   +1 more source

PAX9 Mutation of Non-Syndromic Hypodontia in a Malaysian Family

open access: bronze, 2017
Nur Farahiyah Mohamed Idrus   +5 more
openalex   +2 more sources

Dental Anomalies: Prevalence, Patterns of Association and Relationship With Dental Age. [PDF]

open access: yesInt Dent J
Loscertales-Martín-de-Agar B   +4 more
europepmc   +1 more source

A SCOPING REVIEW: GENE MUTATIONS OF NONSYNDROMIC HYPODONTIA AND ITS PREVALENCE IN GENDER AND TYPE OF TEETH

open access: diamond, 2023
Wan Nur Wanida Wan Saimi   +5 more
openalex   +2 more sources

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