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Conference Paper: Oral manifestation in microcephalic osteodysplastic primordial dwarfism type II: a case report

TitleOral manifestation in microcephalic osteodysplastic primordial dwarfism type II: a case report
Authors
KeywordsMOPD type II
Microdontia
Generalised mobility
Issue Date2013
PublisherWiley-Blackwell Publishing Ltd.. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=0960-7439
Citation
The 24th Congress of the International Association of Pediatric Dentistry, Seoul, Korea, 12-15 June 2013. International Journal of Paediatric Dentistry, 2013, v. 23 suppl. s1, p. 147, abstract P12-310 How to Cite?
AbstractINTRODUCTION: Microcephalic osteodysplastic primordial dwarfism type II (MOPD II) is a rare autosomal recessive inherited form of primordial dwarfism (Kantaputra et al., 2011). Studies suggested this condition is due to mutation of PCNT gen...
DescriptionThis journal suppl. is the Special Issue: Abstracts of the 24th Congress of the International Association of Pediatric Dentistry ... 2013
Poster Session P12 - The Morita Prizes: abstract P12-310
Persistent Identifierhttp://hdl.handle.net/10722/189672
ISSN
2015 Impact Factor: 1.303
2015 SCImago Journal Rankings: 0.721

 

DC FieldValueLanguage
dc.contributor.authorIsmail, AFen_US
dc.contributor.authorYiu, Cen_US
dc.date.accessioned2013-09-17T14:52:46Z-
dc.date.available2013-09-17T14:52:46Z-
dc.date.issued2013en_US
dc.identifier.citationThe 24th Congress of the International Association of Pediatric Dentistry, Seoul, Korea, 12-15 June 2013. International Journal of Paediatric Dentistry, 2013, v. 23 suppl. s1, p. 147, abstract P12-310en_US
dc.identifier.issn0960-7439-
dc.identifier.urihttp://hdl.handle.net/10722/189672-
dc.descriptionThis journal suppl. is the Special Issue: Abstracts of the 24th Congress of the International Association of Pediatric Dentistry ... 2013-
dc.descriptionPoster Session P12 - The Morita Prizes: abstract P12-310-
dc.description.abstractINTRODUCTION: Microcephalic osteodysplastic primordial dwarfism type II (MOPD II) is a rare autosomal recessive inherited form of primordial dwarfism (Kantaputra et al., 2011). Studies suggested this condition is due to mutation of PCNT gen...-
dc.languageengen_US
dc.publisherWiley-Blackwell Publishing Ltd.. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=0960-7439-
dc.relation.ispartofInternational Journal of Paediatric Dentistryen_US
dc.rightsThe definitive version is available at www3.interscience.wiley.com-
dc.subjectMOPD type II-
dc.subjectMicrodontia-
dc.subjectGeneralised mobility-
dc.titleOral manifestation in microcephalic osteodysplastic primordial dwarfism type II: a case reporten_US
dc.typeConference_Paperen_US
dc.identifier.emailYiu, C: ckyyiu@hkucc.hku.hken_US
dc.identifier.authorityYiu, C=rp00018en_US
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1111/ipd.12037-
dc.identifier.hkuros224568en_US
dc.identifier.volume23en_US
dc.identifier.issuesuppl. s1en_US
dc.identifier.spage147en_US
dc.identifier.epage147en_US
dc.publisher.placeUnited Kingdom-
dc.customcontrol.immutablesml 131104-

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