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dentinogenesis imperfecta, imperfect hereditary dentinogenesis相关文献:
Management of Dentinogenesis Imperfecta: A Report of Two Cases.
Kaur A, Kumar S, Karda B, Chibh R.
Int J Clin Pediatr Dent. 2019 Sep-Oct;12(5):464-466. doi: 10.5005/jp-journals-10005-1681.
PMID:32440055
Consanguineous-derived homozygous WNT1 mutation results in osteogenesis imperfect with congenital ptosis and exotropia.
Chen P, Chen J, Yang Z, Lu Y, Shen L, Zhou K, Ye S, Shen B.
Mol Genet Genomic Med. 2020 Aug;8(8):e1350. doi: 10.1002/mgg3.1350. Epub 2020 Jun 11.
PMID:32529806
[Clinical and genetic observations on the hereditary imperfect dentinogenesis].
Firu P, Milicescu V, Negrea A.
Stomatologia (Bucur). 1968 Jan-Feb;15(1):1-10.
PMID:5244029
[Hereditary pathology of the enamel and dentin. A review of molecular genetic research].
Beliakov IuA, Elizarova VM, Krotov VA, Blinnikova OE.
Stomatologiia (Mosk). 2000;79(1):8-9.
PMID:10693338
Brittle teeth with brittle bone in a family for four generations: Case report and literature review.
Shilpa PS, David CM, Kaul R, Sanjay CJ, Narayan BK.
Contemp Clin Dent. 2012 Apr;3(2):197-201. doi: 10.4103/0976-237X.96822.
PMID:22919223
[Oral cavity features in patients suffering from osteogenesis imperfecta].
Alania KN, Iverieli MB, Abashidze NO, Gogishvili KhB, Chigladze TT.
Georgian Med News. 2011 Apr;(193):34-41.
PMID:21617272
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