Publication:
Bilateral absence of maxillary and mandibular second premolars: a clinical, genetic and dermatoglyphic study

dc.contributor.authorsAtasu, M.; Akyüz, S.
dc.date.accessioned2022-03-28T12:45:58Z
dc.date.accessioned2026-01-10T19:02:44Z
dc.date.available2022-03-28T12:45:58Z
dc.date.issued1994
dc.description.abstractIn the report presented here the mode of inheritance pattern of absence of maxillary and mandibular second premolars will be investigated by pedigree analyses and dermatoglyphic studies of a patient who showed the trait and his family members. An 11-year-old male patient with caries with bilateral absence of maxillary and mandibular second premolars was observed. Most of the dermatoglyphic traits observed in the patient were also found in the father and the sister of the patient.
dc.identifier.issn1053-4628
dc.identifier.pubmedPMID: 8054309
dc.identifier.urihttps://hdl.handle.net/11424/255072
dc.language.isoeng
dc.relation.ispartofThe Journal of Clinical Pediatric Dentistry
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectHumans
dc.subjectMale
dc.subjectChild
dc.subjectAnodontia
dc.subjectBicuspid
dc.subjectPedigree
dc.subjectDermatoglyphics
dc.subjectGenes, Dominant
dc.titleBilateral absence of maxillary and mandibular second premolars: a clinical, genetic and dermatoglyphic study
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage221
oaire.citation.startPage219
oaire.citation.titleThe Journal of Clinical Pediatric Dentistry
oaire.citation.volume3

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