[PDF][PDF] Clinical genetic basis of tooth agenesis
M Abu-Hussein, N Watted, M Yehia, P Proff… - Journal of Dental and …, 2015 - aaup.edu
Tooth agenesis is one of the most common congenital malformations in humans.
Hypodontia can either occur as an isolated condition (non-syndromic hypodontia) or can be …
Hypodontia can either occur as an isolated condition (non-syndromic hypodontia) or can be …
New recessive truncating mutation in LTBP3 in a family with oligodontia, short stature, and mitral valve prolapse
SL Dugan, RT Temme, RA Olson… - American Journal of …, 2015 - Wiley Online Library
Latent TGFBbinding protein 3 (LTBP3) is known to increase bioavailability of TGFB. A
homozygous mutation in this gene has previously been associated with oligodontia and …
homozygous mutation in this gene has previously been associated with oligodontia and …
An Aberrant Splice Acceptor Site Due to a Novel Intronic Nucleotide Substitution in MSX1 Gene Is the Cause of Congenital Tooth Agenesis in a Japanese Family
T Tatematsu, M Kimura, M Nakashima, J Machida… - PLoS …, 2015 - journals.plos.org
Congenital tooth agenesis is caused by mutations in the MSX1, PAX9, WNT10A, or AXIN2
genes. Here, we report a Japanese family with nonsyndromic tooth agenesis caused by a …
genes. Here, we report a Japanese family with nonsyndromic tooth agenesis caused by a …
Prevalence and patterns of tooth agenesis in Angle Class II Division 2 malocclusion in Japan
K Ota, K Arai - American Journal of Orthodontics and Dentofacial …, 2015 - Elsevier
Introduction The purpose of this study was to evaluate the prevalence and patterns of tooth
agenesis in subjects with Angle Class II Division 2 malocclusion compared with general …
agenesis in subjects with Angle Class II Division 2 malocclusion compared with general …
[PDF][PDF] Simultaneous occurence of an autosomal dominant inherited MSX1 mutation and an X-linked recessive inherited EDA mutation in one Chinese family with non …
XX Zhang, SW Wong, D Han, HL Feng - Chin J Dent Res, 2015 - researchgate.net
Objective: To describe the simultaneous occurence of an autosomal dominant inherited
MSX1 mutation and an X-linked recessive inherited EDA mutation in one Chinese family …
MSX1 mutation and an X-linked recessive inherited EDA mutation in one Chinese family …
A novel missense mutation in collagenous domain of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia
D Li, R Xu, F Huang, B Wang, Y Tao, Z Jiang, H Li… - Journal of Genetics, 2015 - Springer
XLHED is characterized by sparse hair, abnormal or missing teeth and inability to sweat due
to lack of sweat glands (Zonana 1993). Mutations of EDA gene were identified as causing …
to lack of sweat glands (Zonana 1993). Mutations of EDA gene were identified as causing …
[PDF][PDF] Molekulární a genetické aspekty vzniku nesyndromické ageneze zubů.
L Kramerová, P Krejčí, E Míšová… - Czech Stomatology & …, 2015 - cspzl.dent.cz
SOUHRN Předmět sdělení: Ageneze zubu je nejčastější vývojovou poruchou dentice, kterou
podle databáze Online Mendelian Inheritance in Man (OMIM) nacházíme přibližně u 20 …
podle databáze Online Mendelian Inheritance in Man (OMIM) nacházíme přibližně u 20 …
Застапеност на хиподонцијата кај популацијата во Република Македонија
П Ацев - 2015 - repository.ukim.mk
Hypodontia is a condition at which the patient is missing one or more teeth, due to their
failure to develop. Missing teeth are one of the most common developmental anomalies …
failure to develop. Missing teeth are one of the most common developmental anomalies …