Results 101 to 110 of about 68,540 (292)
Dento-skeletal characteristics of cleft patients with missing teeth
Clinical, Cosmetic and Investigational Dentistry, 2018 Waeil Batwa,1 Hala A Almarhoon,2 Khalid A Almoammar,2 Nasser Alqahtani,2 Sahar F Albarakati,2 Thikriat Al-Jewair3 1Department of Orthodontics, Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia; 2Department of Pediatric Dentistry and ...
Batwa W +5 more
doaj
Cephalometric Soft Tissue Characteristics of Unilateral Cleft Lip and Palate Patients in Relation to Missing Teeth [PDF]
, 2017 Objective. This study aimed to evaluate cephalometric soft tissue characteristics in individuals with unilateral complete cleft lip and palate (UCCLP) both with and without missing teeth. Design.
Hala A. Almarhoon +5 more
core +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide +10 more
wiley +1 more source
Replacing missing or lost teeth [PDF]
The Journal of the American Dental Association, 2021 openaire +2 more sources
Are Environmental Factors Effective in Congenitally Missing Teeth? A Multicenter Study [PDF]
, 2019 Objective: To examine the prevalence of congenital absence of permanent teeth other than third molar teeth in non-syndromic children in the Black Sea and Mediterranean Regions of Turkey, and the correlation between gender and distribution sites in the ...
COŞGUN, ALEM +3 more
core +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT U2 small nuclear RNA auxiliary factor 2 (U2AF2) is an essential pre‐mRNA splicing factor involved in the early stages of pre‐mRNA splicing. To date, multiple individuals have been reported with predominantly heterozygous missense variants presenting intellectual disability, speech and motor delays, seizures, hypotonia, and thin or hypoplastic ...
Amanda Toledo +3 more
wiley +1 more source
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2002 Background and Objective: Congenital missing or absence of one or more teeth is one of anomalies that are mostly seen alone or with hereditary syndromes. Diagnosis of missing can prevent further dento-facial complications. The objective of this study was
M Partovi, P Mehranfar
doaj
International Journal of Vascular Medicine, 2014 Objective. The relationship between oral health and cardiovascular disease is an emerging area of research. The objective of the current study is to evaluate the association of cardiovascular disease and the number of missing teeth as a risk indicator ...
R. Constance Wiener, Usha Sambamoorthi
doaj +1 more source
Concomitant hypo-hyperdontia with dens invaginatus
Indian Journal of Dental Research, 2011 Although developmental anomalies of tooth number are quite common in permanent dentition, concomitant occurrence of hypohyperdontia is a very rare mixed numeric anomalous condition of teeth.
B S Manjunatha +2 more
doaj +1 more source
PUS7 Deficiency: Phenotypical Expansion of PUS7‐Related Neurodevelopmental Disorders
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Pathogenic variants in PUS7, encoding pseudouridine synthase 7, cause a rare neurodevelopmental disorder marked by intellectual disability, microcephaly, short stature, and behavioral disturbances. Since the first report in 2018, only 16 patients have been described.
Alice Muda +5 more
wiley +1 more source