12664252

Source:http://linkedlifedata.com/resource/pubmed/id/12664252

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008029, umls-concept:C0015576, umls-concept:C0079411, umls-concept:C0086345, umls-concept:C0205210, umls-concept:C0302523, umls-concept:C0700325
pubmed:issue	2
pubmed:dateCreated	2003-3-28
pubmed:abstractText	Cherubism is a rare fibro-osseous disorder that almost exclusively affects the maxilla and mandible.
pubmed:language	ger
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9716576
pubmed:citationSubset	D
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/FGFR3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Tyrosine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Fibroblast Growth..., http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Fibroblast Growth Factor
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1432-9417
pubmed:author	pubmed-author:BillJ SJS, pubmed-author:HoffmeisterBB, pubmed-author:OpitzCC, pubmed-author:PetersHH, pubmed-author:PetschlerMM, pubmed-author:StillerMM, pubmed-author:WitkowskiRR
pubmed:issnType	Print
pubmed:volume	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	83-7
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:12664252-Adolescent, pubmed-meshheading:12664252-Adult, pubmed-meshheading:12664252-Cherubism, pubmed-meshheading:12664252-Child, pubmed-meshheading:12664252-Child, Preschool, pubmed-meshheading:12664252-Chromosome Aberrations, pubmed-meshheading:12664252-Chromosomes, Human, Pair 4, pubmed-meshheading:12664252-Combined Modality Therapy, pubmed-meshheading:12664252-Craniosynostoses, pubmed-meshheading:12664252-Female, pubmed-meshheading:12664252-Follow-Up Studies, pubmed-meshheading:12664252-Genes, Dominant, pubmed-meshheading:12664252-Genetic Predisposition to Disease, pubmed-meshheading:12664252-Humans, pubmed-meshheading:12664252-Infant, pubmed-meshheading:12664252-Male, pubmed-meshheading:12664252-Orthodontics, Corrective, pubmed-meshheading:12664252-Osteoarthropathy, Secondary Hypertrophic, pubmed-meshheading:12664252-Pedigree, pubmed-meshheading:12664252-Protein-Tyrosine Kinases, pubmed-meshheading:12664252-Receptor, Fibroblast Growth Factor, Type 3, pubmed-meshheading:12664252-Receptors, Fibroblast Growth Factor, pubmed-meshheading:12664252-Tooth Abnormalities
pubmed:year	2003
pubmed:articleTitle	[Clinical and molecular genetic observations on families with cherubism over three generations].
pubmed:affiliation	Abteilung für Zahnärztliche Chirurgie und Röntgenologie, Klinik für Kieferchirugie und plastische Gesichtschirurgie, Universitätsklinikum Benjamin Franklin, Berlin. michael.petschler@ukbf.fu-berlin.de
pubmed:publicationType	Journal Article, English Abstract, Case Reports