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Facial dysmorphism, multiple pigmented nevi, osteoporosis, brachydactyly, and other skeletal changes in a male: a new syndrome?

dc.contributor.authorSaglam, M
dc.contributor.authorUlucan, H
dc.contributor.authorGul, D
dc.contributor.authorOktenli, C
dc.date.accessioned2021-03-03T10:33:21Z
dc.date.available2021-03-03T10:33:21Z
dc.date.issued2003
dc.identifier.citationOktenli C., Ulucan H., Saglam M., Gul D., "Facial dysmorphism, multiple pigmented nevi, osteoporosis, brachydactyly, and other skeletal changes in a male: a new syndrome?", CLINICAL DYSMORPHOLOGY, cilt.12, sa.2, ss.149-151, 2003
dc.identifier.issn0962-8827
dc.identifier.othervv_1032021
dc.identifier.otherav_2334aee0-92dd-46f5-971d-f6abc0ba27cb
dc.identifier.urihttp://hdl.handle.net/20.500.12627/28643
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/12868484
dc.identifier.urihttps://doi.org/10.1097/01.mcd.0000052340.43310.a7
dc.description.abstractA adult male is described with facial dysmorphism, multiple pigmented nevi, osteoporosis, and multiple skeletal anomalies. This combination does not fit any known syndromes and may represent a new entity.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTıp
dc.subjectGENETİK VE HAYAT
dc.titleFacial dysmorphism, multiple pigmented nevi, osteoporosis, brachydactyly, and other skeletal changes in a male: a new syndrome?
dc.typeMakale
dc.relation.journalCLINICAL DYSMORPHOLOGY
dc.contributor.department, ,
dc.identifier.volume12
dc.identifier.issue2
dc.identifier.startpage149
dc.identifier.endpage151
dc.contributor.firstauthorID727244


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