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PUBMED FOR HANDHELDS

Journal Abstract Search


82 related items for PubMed ID: 194340

  • 1. [Oculodentodigitaldysplasia].
    Fára M, Horák I, Hrivnáková J, Kapras J, Nová M, Stloukalová M.
    Rozhl Chir; 1977 Feb; 56(2):129-38. PubMed ID: 194340
    [No Abstract] [Full Text] [Related]

  • 2. Generalised hypomineralisation of enamel in oculodentodigital dysplasia: comprehensive dental management of a case.
    Jensen ED.
    BMJ Case Rep; 2021 Jan 11; 14(1):. PubMed ID: 33431460
    [Abstract] [Full Text] [Related]

  • 3. [An unexplained syndrom with eye and tooth defects (author's transl)].
    Schäfer WD, Schell-Wölker H.
    Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1974 Jan 11; 191(3):197-210. PubMed ID: 4153171
    [No Abstract] [Full Text] [Related]

  • 4. [4 cases of oculodentodigital syndrome].
    Yoshino S, Yamauchi Y, Mikami R.
    Seikei Geka; 1968 Jan 11; 19(2):91-2. PubMed ID: 4300322
    [No Abstract] [Full Text] [Related]

  • 5. The oral manifestations of trisomy G-1 (Down syndrome).
    Cohen MM, Cohen MM.
    Birth Defects Orig Artic Ser; 1971 Jun 11; 7(7):241-51. PubMed ID: 4281324
    [No Abstract] [Full Text] [Related]

  • 6. Dental developmental disturbances in 50 individuals with the 22q11.2 deletion syndrome; relation to medical conditions?
    Nordgarden H, Lima K, Skogedal N, Følling I, Storhaug K, Abrahamsen TG.
    Acta Odontol Scand; 2012 May 11; 70(3):194-201. PubMed ID: 22070626
    [Abstract] [Full Text] [Related]

  • 7. A rare symptom of a very rare disease: a case report of a oculodentodigital dysplasia with lymphedema.
    Gumus E.
    Clin Dysmorphol; 2018 Jul 11; 27(3):91-93. PubMed ID: 29624507
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
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  • 9. [Association of ectodermal dysplasia and syndactylia].
    Boudghene-Stambouli O, Merad-Boudia A.
    Ann Dermatol Venereol; 1991 Jul 11; 118(2):107-10. PubMed ID: 1646587
    [No Abstract] [Full Text] [Related]

  • 10. Oculodentodigital dysplasia syndrome. Report of four cases.
    Thodén CJ, Ryöppy S, Kuitunen P.
    Acta Paediatr Scand; 1977 Sep 11; 66(5):635-8. PubMed ID: 197779
    [Abstract] [Full Text] [Related]

  • 11. [Two new cases of the oculo-dento-digital syndrome (author's transl)].
    Levai JP, Cisterne JP, Malpuech G, Fourrier P.
    Ann Chir; 1979 Sep 11; 33(9):739-40. PubMed ID: 232647
    [No Abstract] [Full Text] [Related]

  • 12. Enamel defects in a case of Menkes' syndrome.
    Pallotta R, Del Rosso F, Domizio S, Carlone G, Petrucci A.
    Acta Stomatol Belg; 1989 Jun 11; 86(1):33-6. PubMed ID: 2801367
    [Abstract] [Full Text] [Related]

  • 13. Oculodentodigital dysplasia.
    Farman AG, Smith SN, Nortjé CJ.
    Br Dent J; 1977 Jun 21; 142(12):405-8. PubMed ID: 406906
    [No Abstract] [Full Text] [Related]

  • 14. Otodental syndrome: a case report.
    Colter JD, Sedano HO.
    Pediatr Dent; 2005 Jun 21; 27(6):482-5. PubMed ID: 16532889
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Oculodentodigital dysplasia: ulnar-sided syndactyly and its associated disorders.
    Jones C, Baldrighi C, Mills J, Bush P, Ezaki M, Oishi S.
    J Hand Surg Am; 2011 Nov 21; 36(11):1816-21. PubMed ID: 22036282
    [Abstract] [Full Text] [Related]

  • 17. The question of hypertelorism in oculodentoosseous dysplasia.
    Fará M, Gorlin RJ.
    Am J Med Genet; 1981 Nov 21; 10(1):101-2. PubMed ID: 6794368
    [No Abstract] [Full Text] [Related]

  • 18. [Clinical and genetic contribution to the orofacialdigital syndrome].
    Wiemann C, Witkowski R.
    Padiatr Grenzgeb; 1968 Nov 21; 7(2):85-94. PubMed ID: 4304636
    [No Abstract] [Full Text] [Related]

  • 19.
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  • 20. Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the connexin 43 gene.
    van Es RJ, Wittebol-Post D, Beemer FA.
    Int J Oral Maxillofac Surg; 2007 Sep 21; 36(9):858-60. PubMed ID: 17509830
    [Abstract] [Full Text] [Related]


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