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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 27500518)

  • 1. Cleidocranial Dysplasia with 6p21.1-p12.3 Microdeletion: A Case Report and Literature Review.
    Puvabanditsin S; February M; Mayne J; McConnell J; Mehta R
    Cleft Palate Craniofac J; 2018 Jul; 55(6):891-894. PubMed ID: 27500518
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic mapping of the cleidocranial dysplasia (CCD) locus on chromosome band 6p21 to include a microdeletion.
    Gelb BD; Cooper E; Shevell M; Desnick RJ
    Am J Med Genet; 1995 Aug; 58(2):200-5. PubMed ID: 8533817
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanning RUNX2 and VEGF.
    Izumi K; Yahagi N; Fujii Y; Higuchi M; Kosaki R; Naito Y; Nishimura G; Hosokai N; Takahashi T; Kosaki K
    Am J Med Genet A; 2006 Feb; 140(4):398-401. PubMed ID: 16419134
    [No Abstract]   [Full Text] [Related]  

  • 4. 6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delay.
    Chen CP; Lin SP; Liu YP; Chern SR; Wu PS; Chen YT; Su JW; Lee CC; Wang W
    Gene; 2013 Jul; 523(1):99-102. PubMed ID: 23578800
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel Alu-mediated microdeletion in the RUNX2 gene in a Chinese patient with cleidocranial dysplasia.
    Qian Y; Zhang Y; Wei B; Zhang M; Yang J; Leng C; Ge Z; Xu X; Sun M
    J Genet; 2018 Mar; 97(1):137-143. PubMed ID: 29666333
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literature.
    Fernandez BA; Siegel-Bartelt J; Herbrick JA; Teshima I; Scherer SW
    Clin Genet; 2005 Oct; 68(4):349-59. PubMed ID: 16143022
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.
    Purandare SM; Mendoza-Londono R; Yatsenko SA; Napierala D; Scott DA; Sibai T; Casas K; Wilson P; Lee J; Muneer R; Leonard JC; Ramji FG; Lachman R; Li S; Stankiewicz P; Lee B; Mulvihill JJ
    Am J Med Genet A; 2008 Feb; 146A(4):453-8. PubMed ID: 18203189
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel mutation of gene CBFA1/RUNX2 in cleidocranial dysplasia.
    Lo Muzio L; Tetè S; Mastrangelo F; Cazzolla AP; Lacaita MG; Margaglione M; Campisi G
    Ann Clin Lab Sci; 2007; 37(2):115-20. PubMed ID: 17522365
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family.
    Mundlos S; Mulliken JB; Abramson DL; Warman ML; Knoll JH; Olsen BR
    Hum Mol Genet; 1995 Jan; 4(1):71-5. PubMed ID: 7711736
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 115(6):e440-e444. PubMed ID: 29087131
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Genetic analysis of a child with cleidocranial dysplasia and 6q21-q22.31 microdeletion].
    Wu D; Li T; Hou Q; Huo X; Wang X; Wang T; Yang Y; Liu H; Liao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):253-256. PubMed ID: 29653004
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.
    Jaruga A; Hordyjewska E; Kandzierski G; Tylzanowski P
    Clin Genet; 2016 Nov; 90(5):393-402. PubMed ID: 27272193
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.
    Innis JW; Asher JH; Liang Y; Wang A; Wilke CM; Dierick HA; Kazen-Gillespie K; Sheldon S; Glover TW; Friedman TB
    Am J Med Genet; 1997 Aug; 71(3):292-7. PubMed ID: 9268099
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia.
    Northup JK; Matalon R; Lockhart LH; Hawkins JC; Velagaleti GV
    Eur J Med Genet; 2011; 54(4):e394-8. PubMed ID: 21466863
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2.
    El-Gharbawy AH; Peeden JN; Lachman RS; Graham JM; Moore SR; Rimoin DL
    Am J Med Genet A; 2010 Jan; 152A(1):169-74. PubMed ID: 20014132
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 11(3):301-305. PubMed ID: 30468148
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cleidocranial dysplasia: clinical and molecular genetics.
    Mundlos S
    J Med Genet; 1999 Mar; 36(3):177-82. PubMed ID: 10204840
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in the RUNX2 gene in patients with cleidocranial dysplasia.
    Otto F; Kanegane H; Mundlos S
    Hum Mutat; 2002 Mar; 19(3):209-16. PubMed ID: 11857736
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 528():6-12. PubMed ID: 35065050
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.