Results 61 to 70 of about 556 (151)
Case Reports in Dentistry, Volume 2012, Issue 1, 2012., 2012 The Gorlin‐Goltz syndrome (GGS) (the nevoid basal cell carcinoma syndrome—NBCCS) is a rare autosomal dominant syndrome caused due to mutations in the PTCH (patched) gene found on chromosome arm 9q. The syndrome, characterized by increased predisposition to develop basal cell carcinoma and associated multiorgan anomalies, has a high level of penetrance ...
Padma Pandeshwar +4 more
wiley +1 more source
An enigmatic teleost fish from the Eocene of Bolca (Italy) with unusual larval‐like features
Papers in Palaeontology, Volume 11, Issue 3, May/June 2025.Abstract ‘Pegasus’ volans is a highly unusual fossil teleost fish from the celebrated Eocene Bolca Lagerstätte. The fossil, known on the basis of two specimens, has been historically assigned to seamoths (Pegasidae), then to oarfishes and relatives (Lampriformes).
Donald Davesne, Giorgio Carnevale
wiley +1 more source
Evidence‐Based Anatomical Terminology in Dentistry Developed by a Consortium of Experts
Clinical Anatomy, Volume 38, Issue 3, Page 374-406, April 2025.ABSTRACT This article aimed to develop evidence‐based anatomical terminology in dentistry agreed upon by experts in multiple fields and ultimately to bridge anatomy and clinical dentistry. A comprehensive list of dental anatomical terminology was detailed in table format, and specific terms of interest were highlighted with their respective literature ...
Joe Iwanaga +14 more
wiley +1 more source
The Anatomical Record, Volume 307, Issue 12, Page 3717-3781, December 2024.Abstract Thescelosaurines are a group of early diverging, ornithischian dinosaurs notable for their conservative bauplans and mosaic of primitive features. Although abundant within the latest Cretaceous ecosystems of North America, their record is poor to absent in earlier assemblages, leaving a large gap in our understanding of their evolution ...
Haviv M. Avrahami +3 more
wiley +1 more source
Craniofacial anomalies in a murine model of heterozygous fibroblast growth factor 10 gene mutation
Orthodontics &Craniofacial Research, Volume 27, Issue 1, Page 84-94, February 2024.Abstract Objective Dysregulation of Fibroblast Growth Factor 10 (FGF10), a member of the family of Fibroblast Growth Factor (FGF) proteins, has been implicated in craniofacial and dental anomalies, including craniosynostosis, cleft palate, and Lacrimo‐Auriculo‐Dento‐Digital Syndrome.
Jenny Tan +4 more
wiley +1 more source
Bilateral bifid condyles: A rare etiology of temporomandibular joint disorders.
, 2021 Basckgroud: Bifid mandibular condyle (BMC) is a rare etiology of temporomandibular joint (TMJ) disorders characterized by a duplication of the head of the mandibular condyle.
Duisit, Jérôme +4 more
core +1 more source
Bilateral bifid condyle mandibula features in panoramic radiography: a case report
, 2023 Objectives: The aim of this case report is to describe radiographically the specific features of bifid mandibular condyle that frequently found incidentally on panoramic radiographs.
Gunawan, Gunawan, Fitria, Ivony
core
Tetrafid mandibular condyle: a unique case report and review of the literature
, 2011 Morphological changes such as bifid and trifid mandibular condyle are rare entities. The aim of the present report is to describe a unique morphological variation of the mandibular condyle which has four separate condylar heads (tetrafid mandibular ...
Etoz, O. A. +4 more
core +1 more source
Are the Mallophaga Degenerate Poscids?
, 1902 Psyche: A Journal of Entomology, Volume 9, Issue 313, Page 339-343, 1902.
Vernon L. Kellogg
wiley +1 more source
Bifid mandibular condyle: CT and MR imaging appearance in two patients: case report and review of the literature. [PDF]
AJNR Am J Neuroradiol, 2005 Shriki J +4 more
europepmc +2 more sources