| Genetic craniofacial aberrations. | |
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MedLine Citation:
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PMID: 10066116 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Many craniofacial and dental anomalies have a genetic background. Much research related to the molecular pathology of genetic conditions is being carried out, and new information related to mapping of disease genes, gene identification, and mutations in these genes is accumulating with incredible speed. It is important to be well informed of the molecular background of the conditions that we treat at anomaly clinics. This article reviews the most recent molecular findings related to Turner syndrome, Beckwith-Wiedemann syndrome, Marfan syndrome, Treacher Collins syndrome, cleidocranial dysplasia, and cleft lip and palate. |
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Authors:
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S Pirinen |
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Publication Detail:
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Type: Journal Article; Review |
Journal Detail:
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Title: Acta odontologica Scandinavica Volume: 56 ISSN: 0001-6357 ISO Abbreviation: Acta Odontol. Scand. Publication Date: 1998 Dec |
Date Detail:
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Created Date: 1999-04-28 Completed Date: 1999-04-28 Revised Date: 2005-11-16 |
Medline Journal Info:
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Nlm Unique ID: 0370344 Medline TA: Acta Odontol Scand Country: NORWAY |
Other Details:
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Languages: eng Pagination: 356-9 Citation Subset: D; IM |
Affiliation:
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Institute of Dentistry, Department of Pedodontics and Orthodontics, University of Helsinki, Finland. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Beckwith-Wiedemann Syndrome
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genetics Chromosome Mapping Cleft Lip / genetics Cleft Palate / genetics Cleidocranial Dysplasia / genetics Craniofacial Abnormalities / genetics* Humans Mandibulofacial Dysostosis / genetics Marfan Syndrome / genetics Molecular Biology Mutation / genetics Tooth Abnormalities / genetics Turner Syndrome / genetics |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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