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Journal Abstract Search

221 related items for PubMed ID: 21274329

  • 1. Cleidocranial dysplasia: a case report.
    Karagüzel G, Aktürk FA, Okur E, Gümele HR, Gedik Y, Okten A.
    J Clin Res Pediatr Endocrinol; 2010; 2(3):134-6. PubMed ID: 21274329
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  • 2. A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment.
    Çamtosun E, Akıncı A, Demiral E, Tekedereli İ, Sığırcı A.
    J Clin Res Pediatr Endocrinol; 2019 Sep 03; 11(3):301-305. PubMed ID: 30468148
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  • 3. [Clinical and image features, and identification of pathogenic gene mutation of two cleidocranial dysplasia families].
    Wang GX, Ma LX, Xu WF, Song FL, Sun RP.
    Zhonghua Er Ke Za Zhi; 2010 Nov 03; 48(11):834-8. PubMed ID: 21215027
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  • 4. Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey.
    Berkay EG, Elkanova L, Kalaycı T, Uludağ Alkaya D, Altunoğlu U, Cefle K, Mıhçı E, Nur B, Taşdelen E, Bayramoğlu Z, Karaman V, Toksoy G, Güneş N, Öztürk Ş, Palandüz Ş, Kayserili H, Tüysüz B, Uyguner ZO.
    Am J Med Genet A; 2021 Aug 03; 185(8):2488-2495. PubMed ID: 33987976
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  • 5. 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
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  • 7. Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.
    Jaruga A, Hordyjewska E, Kandzierski G, Tylzanowski P.
    Clin Genet; 2016 Nov 15; 90(5):393-402. PubMed ID: 27272193
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  • 10. [Clinical and molecular study in a family with cleidocranial dysplasia].
    Callea M, Fattori F, Bertini ES, Yavuz I, Bellacchio E, Avendaño A, Araque D, Lacruz-Rengel MA, Da Silva G, Cammarata-Scalisi F.
    Arch Argent Pediatr; 2017 Dec 01; 115(6):e440-e444. PubMed ID: 29087131
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  • 13. Cleidocranial dysplasia with growth hormone deficiency: a case report.
    Takaki N, Mori J, Matsuo S, Osamura T, Michigami T.
    BMC Pediatr; 2020 Jan 16; 20(1):19. PubMed ID: 31948427
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  • 18. Clinical spectrum of cleidocranial dysplasia in a family with twins.
    Wang J, Huang X, Lai C, Jiang K.
    Pediatr Int; 2013 Jun 16; 55(3):392-5. PubMed ID: 23782374
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  • 20. Functional analysis of novel RUNX2 mutations identified in patients with cleidocranial dysplasia.
    Hordyjewska-Kowalczyk E, Sowińska-Seidler A, Olech EM, Socha M, Glazar R, Kruczek A, Latos-Bieleńska A, Tylzanowski P, Jamsheer A.
    Clin Genet; 2019 Nov 16; 96(5):429-438. PubMed ID: 31347140
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