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Oral Diseases, ISSN 1354-523X, 01/2019, Volume 25, Issue 1, pp. 234 - 241
Journal Article
Journal Article
Genetics and Molecular Research, ISSN 1676-5680, 03/2016, Volume 15, Issue 1
Journal Article
Journal of International Society of Preventive & Community Dentistry, ISSN 2231-0762, 05/2015, Volume 5, Issue 3, pp. 170 - 175
Hypodontia is often used as a collective term for congenital absence of primary or secondary teeth, although specifically it describes the absence of one to... 
Studies | Statistical analysis | Classification | Teeth | Aesthetics | Gender | Patients | Orthodontics | Girls | Children & youth | non-syndromic hypodontia | Absence of third molar | orthodontic patient | Original
Journal Article
Cytogenetic and Genome Research, ISSN 1424-8581, 07/2019, Volume 158, Issue 1, pp. 1 - 9
X-linked hypohidrotic ectodermal dysplasia (XLHED; OMIM 305100) is the most common form of ectodermal dysplasia, presenting with the triad of hypotrichosis,... 
Original Article | NON-SYNDROMIC HYPODONTIA | ECTODYSPLASIN-A | WNT10A | EDA | Hypotrichosis | Hypohidrotic ectodermal dysplasia | IDENTIFICATION | FAMILY | CELL BIOLOGY | Ectodysplasin A | GENE | Hypodontia | GENETICS & HEREDITY | MISSENSE MUTATION
Journal Article
Indian Journal of Human Genetics, ISSN 0971-6866, 2013, Volume 19, Issue 4, pp. 459 - 464
Non-syndromic tooth agenesis is a congenital anomaly with significant medical, psychological, and social ramifications. There is sufficient evidence to... 
tooth agenesis | MSX1 mutation | non-syndromic | Tooth diseases | Case studies | Homeobox genes | Genetic aspects | Health aspects | Varieties | Homeotic genes | Original
Journal Article
Journal of Krishna Institute of Medical Sciences University, ISSN 2231-4261, 01/2012, Volume 1, Issue 1, pp. 118 - 121
Background: Concomitant hypo-hyperdontia is an uncommon condition of coexistence of partial anodontia and supernumerary teeth. Its etiology is still unknown.... 
impacted teeth | non syndromic | supernumerary teeth
Journal Article
Journal of Krishna Institute of Medical Sciences University, ISSN 2231-4261, 2012, Volume 1, Issue 1, pp. 118 - 121
Journal Article
by Park, H and Song, JS and Shin, TJ and Hyun, HK and Kim, YJ and Kim, JW
ARCHIVES OF ORAL BIOLOGY, ISSN 0003-9969, 07/2019, Volume 103, pp. 8 - 11
Objectives: To identify the molecular genetic etiology of the families with non-syndromic multiple missing permanent teeth (oligodontia). Materials and... 
WNT10A | ECTODERMAL DYSPLASIA | Whole-exome sequencing | DENTISTRY, ORAL SURGERY & MEDICINE | Non-syndromic | TOOTH AGENESIS | Mutation | PREVALENCE | AXIN2 | Oligodontia | HYPODONTIA
Journal Article
Journal of Orofacial Orthopedics, ISSN 1434-5293, 01/2016, Volume 77, Issue 1, pp. 31 - 38
Journal Article
JOURNAL OF OROFACIAL ORTHOPEDICS-FORTSCHRITTE DER KIEFERORTHOPADIE, ISSN 1434-5293, 03/2017, Volume 78, Issue 2, pp. 112 - 120
The literature suggests an association between phenotype and causative mutation in nonsyndromic oligodontia. Thus, the present study was designed to verify... 
NON-SYNDROMIC OLIGODONTIA | Agenesis | Genotype | Phenotype | AUTOSOMAL-DOMINANT HYPODONTIA | SELECTIVE TOOTH AGENESIS | PERMANENT TEETH | Hypodontia | ECTODERMAL DYSPLASIA | Familial | DENTISTRY, ORAL SURGERY & MEDICINE | MISSENSE MUTATION | PAX9 GENE | Mutation | EDA GENE | NONSENSE MUTATION | MOLAR OLIGODONTIA
Journal Article
JOURNAL OF OROFACIAL ORTHOPEDICS-FORTSCHRITTE DER KIEFERORTHOPADIE, ISSN 1434-5293, 01/2016, Volume 77, Issue 1, pp. 31 - 38
Journal Article
Journal of Dental Research, ISSN 0022-0345, 2/2018, Volume 97, Issue 2, pp. 155 - 162
Tooth agenesis is one of the most common developmental anomalies affecting function and esthetics. The paired-domain transcription factor, Pax9, is critical... 
functional studies | craniofacial anomalies | dental agenesis | oligodontia | craniofacial genetics | phenotypic analysis | NON-SYNDROMIC OLIGODONTIA | POPULATION | WNT10A | METAANALYSIS | INITIATION CODON | PREVALENCE | MISSENSE MUTATIONS | FEATURES | FAMILY | DENTISTRY, ORAL SURGERY & MEDICINE | HYPODONTIA | Research Reports
Journal Article
Genetika, ISSN 0534-0012, 2016, Volume 48, Issue 3, pp. 945 - 954
Selective tooth agenesis is the most common congenital disorder affecting the formation of dentition in humans. Both its forms (hypodontia and more severe... 
Odontogenesis | Oligodontia | Hypodontia | Candidate genes | Genetic causes | NON-SYNDROMIC HYPODONTIA | ISOLATED OLIGODONTIA | WNT10A | AGRONOMY | hypodontia | INHERITED ANOMALIES | oligodontia | AXIN2 POLYMORPHISM | odontogenesis | HYPOHIDROTIC ECTODERMAL DYSPLASIA | candidate genes | DENTAL AGENESIS | PAX9 | GENETICS & HEREDITY | MISSENSE MUTATION | MSX1 | genetic causes
Journal Article
by Song, S and Han, D and Qu, H and Gong, Y and Wu, H and Zhang, X and Zhong, N and Feng, H
Journal of Dental Research, ISSN 0022-0345, 2/2009, Volume 88, Issue 2, pp. 126 - 131
Journal Article
Genes, ISSN 2073-4425, 05/2018, Volume 9, Issue 5, p. 255
Journal Article
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