Results 91 to 100 of about 6,227 (189)

Carrier screening in the reproductive setting—Are there medical implications for the heterozygote?—A guide for clinicians

open access: yesPregnancy, Volume 2, Issue 3, May 2026.
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld   +5 more
wiley   +1 more source

Tooth formation in Sudanese children

open access: yes, 2011
PhDThe aim of this study was to describe the average age of permanent mandibular tooth formation in two groups of Sudanese children using a cross-sectional design following STROBE guidelines.
Elamin, Fadil
core  

Dentofacial Morphology in Third Molar Agenesis [PDF]

open access: yes, 2015
Objective:In the literature, some studies show a relation between tooth agenesis and craniofacial morphology, whereas other authors conclude that dental agenesis exerts little influence on dent facial structures.
Ali ihya Karaman   +4 more
core   +1 more source

Genetic polymorphism in esr2 and risk of tooth agenesis

open access: yesRio de Janeiro Dental Journal (Revista Científica do CRO-RJ), 2019
Introduction: Tooth agenesis (TA) is the congenital absence of teeth. Several studies have proposed a strong genetic background for this condition. Aim: The present cross-sectional study aimed to evaluate whether genetic polymorphisms in the genes that code for estrogen receptors (ESR1 and ESR2) are associated with the presence of isolated TA in a ...
Marañón-Vásquez, Guido Artemio   +7 more
openaire   +2 more sources

Tooth agenesis [PDF]

open access: yesBMJ Case Reports, 2011
Upendra, Jain   +2 more
openaire   +2 more sources

Novel frameshift variant of WNT10A in a Japanese patient with hypodontia

open access: yesHuman Genome Variation
Congenital tooth agenesis is caused by the impairment of crucial genes related to tooth development, such as Wnt signaling pathway genes. Here, we investigated the genetic causes of sporadic congenital tooth agenesis. Exome sequencing, followed by Sanger
Michiyo Ando   +11 more
doaj   +1 more source

Association of AXIN2 gene polymorphisms with nonsyndromic oligodontia in Turkish families

open access: yesDentistry 3000, 2016
Tooth agenesis is the most common developmental abnormality of the human dentition characterized by the congenital absence of one or more permanent teeth.
Nuriye Dinckan   +3 more
doaj   +1 more source

Is Third-Molar Agenesis Related to the Incidence of Other Missing Teeth?

open access: yesTurkish Journal of Orthodontics, 2014
Objective:The aim of this study was to investigate whether third-molar agenesis is related to agenesis of other missing teeth (incisor-premolar hypodontia [IPH]).Materials and Method:A sample of 94 Turkish patients with agenesis of upper lateral incisors
A. Burcu Altan, Ali Altuğ Bıçakçı
doaj   +1 more source

Exploring the Association Between Third Molar Agenesis and Carabelli Traits: A Cross-Sectional Study

open access: yesDentistry Journal
Background/Objectives: Dental agenesis is the congenital absence of at least one tooth and has been associated with several other developmental dental conditions, such as morphological dental alterations and Carabelli trait.
Isabela Ribeiro Madalena   +11 more
doaj   +1 more source

Third molar agenesis among children and youths from three major races of Malaysians

open access: yesJournal of Dental Sciences, 2012
Background/purpose: Third molar (M3) agenesis is linked to the evolution and growth of the human jaw, as it is the last tooth to develop in the human dentition.
Jacob John   +5 more
doaj   +1 more source

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