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Journal Abstract Search

146 related items for PubMed ID: 38737280

  • 1. Prenatal diagnosis of cleidocranial dysplasia: Case report on two cases with a negative family history.
    Han R, Zhang C, Fu X, Zhu Z, Wang X, Li H.
    Heliyon; 2024 May 15; 10(9):e29816. PubMed ID: 38737280
    [Abstract] [Full Text] [Related]

  • 2. 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 May 15; 25(1):36-9. PubMed ID: 19169035
    [Abstract] [Full Text] [Related]

  • 3. A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review.
    Hsueh SJ, Lee NC, Yang SH, Lin HI, Lin CH.
    BMC Neurol; 2017 Jan 06; 17(1):2. PubMed ID: 28056872
    [Abstract] [Full Text] [Related]

  • 4. Novel mutation of RUNX2 gene in a patient with cleidocranial dysplasia.
    Guo YW, Chiu CY, Liu CL, Jap TS, Lin LY.
    Int J Clin Exp Pathol; 2015 Jan 06; 8(1):1057-62. PubMed ID: 25755819
    [Abstract] [Full Text] [Related]

  • 5. Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia.
    Gong L, Odilov B, Han F, Liu F, Sun Y, Zhang N, Zuo X, Yang J, Wang S, Hou X, Ren J.
    Genes Genomics; 2022 Jun 06; 44(6):683-690. PubMed ID: 35235174
    [Abstract] [Full Text] [Related]

  • 6. Cleidocranial Dysplasia: A Clinico-radiographic Spectrum with Differential Diagnosis.
    Patil PP, Barpande SR, Bhavthankar JD, Humbe JG.
    J Orthop Case Rep; 2015 Jun 06; 5(2):21-4. PubMed ID: 27299035
    [Abstract] [Full Text] [Related]

  • 7. Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case.
    Qin XY, Jia PZ, Zhao HX, Li WR, Chen F, Lin JX.
    Chin Med J (Engl); 2017 Jan 20; 130(2):165-170. PubMed ID: 28091408
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Cleidocranial dysplasia: a case report.
    Karagüzel G, Aktürk FA, Okur E, Gümele HR, Gedik Y, Okten A.
    J Clin Res Pediatr Endocrinol; 2010 Sep 03; 2(3):134-6. PubMed ID: 21274329
    [Abstract] [Full Text] [Related]

  • 10. A rare case of cleidocranial dysplasia presenting with failure to thrive.
    Mahajan PS, Mahajan AP, Mahajan PS.
    J Nat Sci Biol Med; 2015 Sep 03; 6(1):232-5. PubMed ID: 25810671
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Genome sequencing identified a novel exonic microdeletion in the RUNX2 gene that causes cleidocranial dysplasia.
    Zhang J, Li YZ, Chen WQ, Yuan JY, Li Q, Meng YX, Yu YD, Guo Q.
    Clin Chim Acta; 2022 Mar 01; 528():6-12. PubMed ID: 35065050
    [Abstract] [Full Text] [Related]

  • 13. An echo-poor spine at 13 weeks: an early sign of cleidocranial dysplasia.
    Hove HD, Hermann NV, Jørgensen C, Kreiborg S, Sundberg K.
    Fetal Diagn Ther; 2008 Mar 01; 24(2):103-5. PubMed ID: 18648208
    [Abstract] [Full Text] [Related]

  • 14. Craniofacial features of cleidocranial dysplasia.
    Pan CY, Tseng YC, Lan TH, Chang HP.
    J Dent Sci; 2017 Dec 01; 12(4):313-318. PubMed ID: 30895069
    [Abstract] [Full Text] [Related]

  • 15. Cleidocranial Dysplasia Presenting With Mixed Dentition in a 28-Year-Old Male: A Case Report.
    Gollapudi M, Mohod S, Mahajan NR, Tiwari AV.
    Cureus; 2024 Jul 01; 16(7):e65273. PubMed ID: 39184626
    [Abstract] [Full Text] [Related]

  • 16. Clinical and radiological findings in a severe case of cleidocranial dysplasia.
    Lotlikar PP, Creanga AG, Singer SR.
    BMJ Case Rep; 2018 Nov 12; 2018():. PubMed ID: 30420564
    [Abstract] [Full Text] [Related]

  • 17. Cleidocranial dysplasia with autosomal dominant inheritance pattern.
    Bhargava P, Khan S, Sharma R, Bhargava S.
    Ann Med Health Sci Res; 2014 Jul 12; 4(Suppl 2):S152-4. PubMed ID: 25184084
    [Abstract] [Full Text] [Related]

  • 18. Parietal aplasia and hypophosphatasia in a child harboring a novel mutation in RUNX2 and a likely pathogenic variant in TNSALP.
    Papadopoulou A, Bountouvi E, Sideri V, Moutsatsou P, Skarakis NS, Doulgeraki A, Karachaliou FE.
    Bone; 2021 May 12; 146():115904. PubMed ID: 33647526
    [Abstract] [Full Text] [Related]

  • 19. RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia.
    Lin WD, Lin SP, Wang CH, Tsai Y, Chen CP, Tsai FJ.
    Genet Mol Biol; 2011 Apr 12; 34(2):201-4. PubMed ID: 21734816
    [Abstract] [Full Text] [Related]

  • 20. Cleidocranial dysplasia (CCD) causing respiratory distress syndrome in a newborn infant. A case report.
    Ringe KI, Schirg E, Galanski M.
    J Radiol Case Rep; 2010 Apr 12; 4(4):9-12. PubMed ID: 22470720
    [Abstract] [Full Text] [Related]

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