Results 201 to 210 of about 6,152 (269)
A novel PAX9 variant in a Chinese family with non-syndromic oligodontia and genotype-phenotype analysis of PAX9variants. [PDF]
Zhanyun Jin +14 more
openalex +1 more source
Treatment of a Patient with Oligodontia: A Case Report
Nursel Akkaya +2 more
openalex +1 more source
A Case of FAM111A-Associated Kenny-Caffey Syndrome Type 2 with New Clinical Features: Microtia, Lacunar Skull Appearance, and Arnold-Chiari Malformation. [PDF]
Doğan Arı AB +4 more
europepmc +1 more source
Expanding the Mutational Spectrum of TSPEAR in Ectodermal Dysplasia Type 14: A Familial Case Study. [PDF]
Sirica R +12 more
europepmc +1 more source
Enamel hypoplasia with nonsyndromic oligodontia: A rare case report. [PDF]
Pracheth TV +3 more
europepmc +1 more source
Graduate School of Biomedical Sciences, University of Texas Health Science Center at Houston/M.D. Anderson Cancer Center
core +1 more source
Longitudinal follow up of a boy affected by Pol III-related leukodystrophy: a detailed phenotype description [PDF]
core +1 more source
Dental Management of Ectodermal Dysplasia: A Report of Two Clinical Cases. [PDF]
Elgasmi FE +3 more
europepmc +1 more source

