Results 131 to 140 of about 8,363 (211)

A novel pathogenic mutation in TSPEAR associated with sensorineural hearing loss: a case report and review of the literature. [PDF]

J Med Case Rep
Ahmadkhani A, Taherifard E, Zoghi S, Jafari Khamirani H, Ahmadkhani M, Dastgheib SA.   +5 more
europepmc   +1 more source

Dental Anomalies: Prevalence, Patterns of Association and Relationship With Dental Age. [PDF]

Int Dent J
Loscertales-Martín-de-Agar B, Cabezas-Corado Á, Baus-Domínguez M, Loscertales-Abril J, Torres-Lagares D.   +4 more
europepmc   +1 more source

Expanding the Genotype Spectrum- A Novel POLR3B Variant in 4H Leukodystrophy. [PDF]

Ann Indian Acad Neurol
Sachithanandan S, Krishnan S, Urulangodi M, Puthenveedu DK, Vijayaraghavan A.   +4 more
europepmc   +1 more source

Hypodontia in a child with keratitis-ichthyosis-deafness (KID) syndrome: a case report. [PDF]

J Med Case Rep
Saleh TS, Poulsen T, Nyman JE.
europepmc   +1 more source

Influences of genetic and environmental factors on developmental dental anomalies: a twin study. [PDF]

BMC Oral Health
Budak I, Oz E.
europepmc   +1 more source

Dermatoglyphics and Hypodontia

Iranian Journal of Pediatric Dentistry, 2016
B Ajami, N Mahdavi shahri, M Ebrahimi, N GHavide   +3 more
openaire   +1 more source

Oral Manifestations in Adolescents with Genetic Syndromes: A Retrospective Cross-Sectional Study. [PDF]

J Clin Med
Țenț A, Iurcov R, Moca AE, Moca RT, Țig IA, Matei RI.   +5 more
europepmc   +1 more source

Prevalence and Associated Factors of Specific Dentofacial Characteristics in Saudi Populations: A Systematic Review and Meta-Analysis. [PDF]

Cureus
Zailai A, Mubarki O, Masoud MA, Majrashi MH, Alhazmi A, Alqurayshah MM, Alotaibi NA, Alotaibi TN, Abusharha AA, Adawi AA, Algashesh JI, Almajhad RI, AlSaeed HA, Alshammari KF.   +13 more
europepmc   +1 more source

A classical variant of ectodermal dysplasia: a case report. [PDF]

Pan Afr Med J
Jawade S, Wankhede P, Sharma R, Munjewar P, More V.   +4 more
europepmc   +1 more source

A certain set of signs that could be compatible with Kabuki syndrome: a case report of an Iranian girl and review of literature. [PDF]

J Med Case Rep
Owlia F, Irannezhad M, Bahrololoomi Z, Mosallaeipour S.   +3 more
europepmc   +1 more source