Publication:
Local, hypoplastic type of amelogenesis imperfecta: a clinical, genetic, radiological and dermatoglyphic study

dc.contributor.authorsAtasu, M.; Genc, A.; Namdar, F.
dc.date.accessioned2022-03-28T12:45:39Z
dc.date.accessioned2026-01-10T17:16:16Z
dc.date.available2022-03-28T12:45:39Z
dc.date.issued1996
dc.description.abstractA patient and her family members showing X-linked dominant form local, hypoplastic type of amelogenesis imperfecta (AI) were investigated from view-point of their teeth, clinical, genetic, radiological and particularly dermatoglyphic findings. It was suggested that it might be a close relationship between the intra-uterine development of both AI and unusual dermatoglyphs originated from the same layer, ectoderm and an X-linked dominant gene could determine both abnormal teeth and unusual dermatoglyphic characteristics in questions.
dc.identifier.issn1053-4628
dc.identifier.pubmedPMID: 9151630
dc.identifier.urihttps://hdl.handle.net/11424/254956
dc.language.isoeng
dc.relation.ispartofThe Journal of Clinical Pediatric Dentistry
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectHumans
dc.subjectAdolescent
dc.subjectPedigree
dc.subjectDermatoglyphics
dc.subjectAmelogenesis Imperfecta
dc.subjectEctoderm
dc.subjectGenetic Linkage
dc.subjectX Chromosome
dc.titleLocal, hypoplastic type of amelogenesis imperfecta: a clinical, genetic, radiological and dermatoglyphic study
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage342
oaire.citation.startPage337
oaire.citation.titleThe Journal of Clinical Pediatric Dentistry
oaire.citation.volume4

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