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Journal Abstract Search

116 related items for PubMed ID: 12822083

  • 41. [Cleidocranial dysplasia. Report of 3 new cases].
    Querin F, Galassi G, Quadu G.
    Radiol Med; 1987; 73(1-2):105-8. PubMed ID: 3809624
    [No Abstract] [Full Text] [Related]

  • 42. Prenatal 3D ultrasound diagnostics in cleidocranial dysplasia.
    Hermann NV, Hove HD, Jørgensen C, Larsen P, Darvann TA, Kreiborg S, Sundberg K.
    Fetal Diagn Ther; 2009; 25(1):36-9. PubMed ID: 19169035
    [Abstract] [Full Text] [Related]

  • 43. A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia.
    Tsai FJ, Wu JY, Lin WD, Tsai CH.
    Acta Paediatr; 2000 Oct; 89(10):1262-5. PubMed ID: 11083386
    [No Abstract] [Full Text] [Related]

  • 44. Clinical spectrum of cleidocranial dysplasia in a family with twins.
    Wang J, Huang X, Lai C, Jiang K.
    Pediatr Int; 2013 Jun; 55(3):392-5. PubMed ID: 23782374
    [Abstract] [Full Text] [Related]

  • 45. 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; 18(2):184-90. PubMed ID: 22023169
    [Abstract] [Full Text] [Related]

  • 46. [Rare disorder in the cranial ossification with a hereditary autosomal dominant character].
    Srsen S, Lányi A.
    Cesk Pediatr; 1972 Dec; 27(12):590 passim. PubMed ID: 4642904
    [No Abstract] [Full Text] [Related]

  • 47. Prenatal sonographic diagnosis of cleidocranial dysostosis.
    Hassan J, Sepulveda W, Teixeira J, Garrett C, Fisk NM.
    Prenat Diagn; 1997 Aug; 17(8):770-2. PubMed ID: 9267902
    [Abstract] [Full Text] [Related]

  • 48. [Cleidocranial dysplasia].
    Fragoso R, Martínez Basalo C, Hernández A, Nazara Z, Martínez y Martínez R, María Cantú J.
    Bol Med Hosp Infant Mex; 1980 Aug; 37(2):325-31. PubMed ID: 7378182
    [Abstract] [Full Text] [Related]

  • 49.
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  • 50. Cleidocranial dysplasia: radiological appearances on dental panoramic radiography.
    McNamara CM, O'Riordan BC, Blake M, Sandy JR.
    Dentomaxillofac Radiol; 1999 Mar; 28(2):89-97. PubMed ID: 10522197
    [Abstract] [Full Text] [Related]

  • 51. Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia.
    Ott CE, Leschik G, Trotier F, Brueton L, Brunner HG, Brussel W, Guillen-Navarro E, Haase C, Kohlhase J, Kotzot D, Lane A, Lee-Kirsch MA, Morlot S, Simon ME, Steichen-Gersdorf E, Tegay DH, Peters H, Mundlos S, Klopocki E.
    Hum Mutat; 2010 Aug; 31(8):E1587-93. PubMed ID: 20648631
    [Abstract] [Full Text] [Related]

  • 52.
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  • 53. Delayed dental maturation in cleidocranial dysplasia.
    Shaikh R, Shusterman S.
    ASDC J Dent Child; 1998 Aug; 65(5):325-9, 355. PubMed ID: 9795736
    [Abstract] [Full Text] [Related]

  • 54. Hypophosphatasia and cleidocranial dysplasia-a case report and review of the literature: the role of the neurosurgeon.
    Blionas A, Friehs GM, Zerris VA.
    Childs Nerv Syst; 2022 Feb; 38(2):461-464. PubMed ID: 34131769
    [Abstract] [Full Text] [Related]

  • 55.
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  • 56. Early prenatal ultrasound diagnosis of cleidocranial dysplasia.
    Stewart PA, Wallerstein R, Moran E, Lee MJ.
    Ultrasound Obstet Gynecol; 2000 Feb; 15(2):154-6. PubMed ID: 10776001
    [Abstract] [Full Text] [Related]

  • 57. [Cleidocranial dysostosis: a clinicoradiologic study of 2 sisters].
    Adami-Lami Conti C, Corti P, Aulisi A, Nistri R, Fantacci C, Calandi C.
    Radiol Med; 1980 Oct; 66(10):713-5. PubMed ID: 7221032
    [No Abstract] [Full Text] [Related]

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