Results 151 to 160 of about 2,544 (214)

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

open access: yesJ Med Case Rep
Ahmadkhani A   +5 more
europepmc   +1 more source

Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies. [PDF]

open access: yesInt J Mol Sci
Ruangchan C   +15 more
europepmc   +1 more source

Silver-Russell syndrome: phenotype features and oral health status. [PDF]

open access: yesOrphanet J Rare Dis
Piekoszewska-ZiÄ™tek P   +4 more
europepmc   +1 more source

Genotype-phenotype analysis and functional study of three novel <i>LRP6</i> variants in non-syndromic oligodontia. [PDF]

open access: yesFront Genet
Yuan Y   +12 more
europepmc   +1 more source

Dental Anomalies in Saudi Arabia: A Systematic Review. [PDF]

open access: yesHealthcare (Basel)
Aljohani K   +3 more
europepmc   +1 more source

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