These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

200 related items for PubMed ID: 10416150

  • 1. Anomalies of craniofacial skeleton and teeth in cleidocranial dysplasia.
    Kreiborg S, Jensen BL, Larsen P, Schleidt DT, Darvann T.
    J Craniofac Genet Dev Biol; 1999; 19(2):75-9. PubMed ID: 10416150
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. RUNX2 mutations in cleidocranial dysplasia.
    Lee KE, Seymen F, Ko J, Yildirim M, Tuna EB, Gencay K, Kim JW.
    Genet Mol Res; 2013 Oct 15; 12(4):4567-74. PubMed ID: 24222232
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Delayed diagnosis of cleidocranial dysplasia in an adult: a case report.
    Gömleksiz C, Arslan E, Arslan S, Pusat S, Arslan EA.
    Acta Med Acad; 2014 Oct 15; 43(1):92-6. PubMed ID: 24893645
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. A 13-year-old Caucasian boy with cleidocranial dysplasia: a case report.
    Kolokitha OE, Ioannidou I.
    BMC Res Notes; 2013 Jan 05; 6():6. PubMed ID: 23289840
    [Abstract] [Full Text] [Related]

  • 9. Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.
    Lee B, Thirunavukkarasu K, Zhou L, Pastore L, Baldini A, Hecht J, Geoffroy V, Ducy P, Karsenty G.
    Nat Genet; 1997 Jul 05; 16(3):307-10. PubMed ID: 9207800
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report.
    Inchingolo AD, Patano A, Coloccia G, Ceci S, Inchingolo AM, Marinelli G, Malcangi G, Montenegro V, Laudadio C, Palmieri G, Bordea IR, Ponzi E, Orsini P, Ficarella R, Scarano A, Lorusso F, Dipalma G, Corsalini M, Gentile M, Venere DD, Inchingolo F.
    Medicina (Kaunas); 2021 Dec 10; 57(12):. PubMed ID: 34946295
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Cleidocranial dysplasia: oral features and genetic analysis of 11 patients.
    Bufalino A, Paranaíba LM, Gouvêa AF, Gueiros LA, Martelli-Júnior H, Junior JJ, Lopes MA, Graner E, De Almeida OP, Vargas PA, Coletta RD.
    Oral Dis; 2012 Mar 10; 18(2):184-90. PubMed ID: 22023169
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Severe cleidocranial dysplasia can mimic hypophosphatasia.
    Unger S, Mornet E, Mundlos S, Blaser S, Cole DE.
    Eur J Pediatr; 2002 Nov 10; 161(11):623-6. PubMed ID: 12424591
    [Abstract] [Full Text] [Related]

  • 18. Cleidocranial dysplasia: report of 3 cases and literature review.
    Shen Z, Zou CC, Yang RW, Zhao ZY.
    Clin Pediatr (Phila); 2009 Mar 10; 48(2):194-8. PubMed ID: 18832541
    [Abstract] [Full Text] [Related]

  • 19. Cleidocranial dysplasia: a case report.
    Karagüzel G, Aktürk FA, Okur E, Gümele HR, Gedik Y, Okten A.
    J Clin Res Pediatr Endocrinol; 2010 Mar 10; 2(3):134-6. PubMed ID: 21274329
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.