Pages that link to "Q47244477"
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The following pages link to A unifying aetiological explanation for anomalies of human tooth number and size (Q47244477):
Displaying 50 items.
- 3D-Geomorphometrics tooth shape analysis in hypodontia (Q28658129) (← links)
- Earliest evidence for social endogamy in the 9,000-year-old-population of Basta, Jordan (Q28681552) (← links)
- A curriculum vitae of teeth: evolution, generation, regeneration (Q28760535) (← links)
- Hypodontia: An Update on Its Etiology, Classification, and Clinical Management (Q30234846) (← links)
- Prehistoric health status of the Roonka population (Q30807687) (← links)
- Sequential supernumerary teeth development in a non-syndromic patient; report of a rare case (Q33629308) (← links)
- On the genetics of hypodontia and microdontia: synergism or allelism of major genes in a family with six affected members (Q33683214) (← links)
- Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review (Q33721057) (← links)
- Assessing the association of taurodontism with numeric dentition anomalies in an adult central Indian population (Q34002941) (← links)
- Prevalence of hypodontia in a sample of Sudanese orthodontic patients (Q34069025) (← links)
- Unilateral maxillary canine agenesis: a case report and literature review (Q34080489) (← links)
- Non-invasive endodontic management of fused mandibular second molar and a paramolar, using cone beam computed tomography as an adjunctive diagnostic aid: A case report (Q34241898) (← links)
- Morphogenetic fields within the human dentition: a new, clinically relevant synthesis of an old concept (Q34312475) (← links)
- Genetic and environmental influences on human dental variation: a critical evaluation of studies involving twins (Q34312525) (← links)
- Evidence to suggest that teeth act as human ornament displays signalling mate quality (Q34364589) (← links)
- Hypodontia: genotype or environment? A case report of monozygotic twins (Q34478350) (← links)
- Odontomas and supernumerary teeth: is there a common origin? (Q34550421) (← links)
- Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies (Q34660192) (← links)
- Supernumerary teeth: review of the literature and a survey of 152 cases (Q34744389) (← links)
- PAX9 polymorphisms and susceptibility with sporadic tooth agenesis in Turkish populations: a case-control study (Q35026271) (← links)
- The frequency and characteristics of mesiodens in a Turkish patient population. (Q35108487) (← links)
- Congenitally missing teeth (hypodontia): A review of the literature concerning the etiology, prevalence, risk factors, patterns and treatment (Q35109290) (← links)
- Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region (Q35122484) (← links)
- Meta-analysis and systematic review of factors biasing the observed prevalence of congenitally missing teeth in permanent dentition excluding third molars (Q35263560) (← links)
- Molecular genetics of supernumerary tooth formation (Q35283051) (← links)
- Supernumerary teeth in Indian children: a survey of 300 cases (Q35872358) (← links)
- Dental anomalies in first-degree relatives of transposed canine probands (Q36091788) (← links)
- Assessment of Ethnicity in Indian Population using Tooth Crown Metric Dental Traits (Q36109665) (← links)
- Clinical evaluation of nonsyndromic dental anomalies in Dravidian population: A cluster sample analysis (Q36164073) (← links)
- Bilateral mandibular supernumerary canines: a case report (Q36196243) (← links)
- Cone-beam computed tomography exploration and surgical management of palatal, inverted, and impacted mesiodens (Q36246276) (← links)
- Non-syndromic multiple supernumerary teeth transmitted as an autosomal dominant trait (Q36275597) (← links)
- DNA methylation is critical for tooth agenesis: implications for sporadic non-syndromic anodontia and hypodontia. (Q36497752) (← links)
- Late developing supernumerary premolars: reports of two cases (Q36566065) (← links)
- A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement (Q36577378) (← links)
- The prevalence and distribution of hypodontia in a sample of Qatari patients (Q36651375) (← links)
- Familial human hypodontia--is it all in the genes? (Q36919991) (← links)
- Prevalence of congenitally missing permanent teeth in Iran (Q36954193) (← links)
- Meta-analysis and systematic review of the number of non-syndromic congenitally missing permanent teeth per affected individual and its influencing factors (Q37023486) (← links)
- Clinical and radiological evaluation of inverse impaction of supernumerary teeth (Q37063564) (← links)
- Hypodontia. Does the prevalence and distribution pattern differ in orthodontic patients? (Q37089350) (← links)
- Tooth agenesis: from molecular genetics to molecular dentistry. (Q37198331) (← links)
- Nonsyndromic familial oligodontia with multiple dens invaginatus: a case report of an unusual case (Q37329518) (← links)
- Late-Developing Supernumerary Premolars: Analysis of Different Therapeutic Approaches (Q37330084) (← links)
- Discordant tooth agenesis and peg-shaped in a pair of monozygotic twins: Clinical and molecular study (Q37413854) (← links)
- Multilevel complex interactions between genetic, epigenetic and environmental factors in the aetiology of anomalies of dental development (Q37632772) (← links)
- A multidisciplinary approach for the management of hypodontia: case report. (Q37698763) (← links)
- Presentation of a keratocystic odontogenic tumor with agenesis: a case report (Q37724066) (← links)
- Genetic, environmental and epigenetic influences on variation in human tooth number, size and shape (Q37964496) (← links)
- Paramolar - A supernumerary molar: A case report and an overview (Q38096375) (← links)