[PDF][PDF] Non-syndromic familial hypodontia: rare case reports and literature review

R Mărgărit, OC Andrei, LA Tănăsescu, C Farcaşiu… - Rom J Morphol …, 2019 - rjme.ro
Congenital absence of the teeth, affecting both physiognomy and mastication, can have a
great impact on patients' quality of life. It may appear unilateral or bilateral; frequently, it …

Novel and Private EDA Mutations and Clinical Phenotypes of Korean Patients with X-Linked Hypohidrotic Ectodermal Dysplasia

JS Park, JM Ko, JH Chae - Cytogenetic and Genome Research, 2019 - karger.com
X-linked hypohidrotic ectodermal dysplasia (XLHED; OMIM 305100) is the most common
form of ectodermal dysplasia, presenting with the triad of hypotrichosis, hypodontia, and …

A novel frameshift mutation in the EDA gene in an Iranian patient affected by X-linked hypohidrotic ectodermal dysplasia

M Rahbaran, M Hassani Doabsari… - Cellular & Molecular …, 2019 - Springer
Purpose Ectodermal dysplasias are characterized by developmental abnormalities in
ectodermal structures. Hypohidrotic ectodermal dysplasias (HED) are the most common …

Identification of genes responsible for the variation in facial and teeth morphology in Latin Americans

M Fuentes-Guajardo - 2019 - discovery.ucl.ac.uk
Facial and dental features are of considerable importance in biomedicine and forensics.
Facial appearance has a strong genetic component and could have evolved to facilitate …

Next generation sequencing approaches in rare diseases: the study of four different families

ML Genovesi - 2019 - iris.uniroma1.it
The main purpose of this PhD project was to study the molecular bases of rare Mendelian
diseases through Next Generation Sequencing (NGS), finding the most appropriate NGS …

[引用][C] Oligodontili çocukların dişsel özelliklerinin ve yaşam kalitesinin değerlendirilmesi

C Bayraktar - platform.almanhal.com
Al Manhal Platform The session has been expired. Please reload the page Reload Please
wait... The file is being prepared Preview Mode If you would like full access to this publication …