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.
230 related articles for article (PubMed ID: 29058294)
1. A novel gene mutation of Runx2 in cleidocranial dysplasia. Peng YJ; Chen QY; Fu DJ; Liu ZM; Mao TT; Li J; She WT J Huazhong Univ Sci Technolog Med Sci; 2017 Oct; 37(5):772-776. PubMed ID: 29058294 [TBL] [Abstract][Full Text] [Related]
2. Novel RUNX2 mutations in Chinese individuals with cleidocranial dysplasia. Zhang CY; Zheng SG; Wang YX; Zhu JX; Zhu X; Zhao YM; Ge LH J Dent Res; 2009 Sep; 88(9):861-6. PubMed ID: 19767586 [TBL] [Abstract][Full Text] [Related]
3. A novel small deletion mutation in RUNX2 gene in one Chinese family with cleidocranial dysplasia. Chen T; Hou J; Hu LL; Gao J; Wu BL Int J Clin Exp Pathol; 2014; 7(5):2490-5. PubMed ID: 24966961 [TBL] [Abstract][Full Text] [Related]
4. A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia. Xu W; Chen Q; Liu C; Chen J; Xiong F; Wu B BMC Med Genet; 2017 Feb; 18(1):13. PubMed ID: 28173761 [TBL] [Abstract][Full Text] [Related]
5. [Mutation analysis of the RUNX2 gene in a family with cleidocranial dysplasia]. Jiang T; Jiang X; Zhang Y Hua Xi Kou Qiang Yi Xue Za Zhi; 2013 Oct; 31(5):522-5. PubMed ID: 24298808 [TBL] [Abstract][Full Text] [Related]
6. Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype. Kim HJ; Nam SH; Kim HJ; Park HS; Ryoo HM; Kim SY; Cho TJ; Kim SG; Bae SC; Kim IS; Stein JL; van Wijnen AJ; Stein GS; Lian JB; Choi JY J Cell Physiol; 2006 Apr; 207(1):114-22. PubMed ID: 16270353 [TBL] [Abstract][Full Text] [Related]
8. A novel 18-bp in-frame deletion mutation in RUNX2 causes cleidocranial dysplasia. Zeng L; Wei J; Zhao N; Sun S; Wang Y; Feng H Arch Oral Biol; 2018 Dec; 96():243-248. PubMed ID: 29089101 [TBL] [Abstract][Full Text] [Related]
9. A novel RUNX2 missense mutation predicted to disrupt DNA binding causes cleidocranial dysplasia in a large Chinese family with hyperplastic nails. Tang S; Xu Q; Xu X; Du J; Yang X; Jiang Y; Wang X; Speck N; Huang T BMC Med Genet; 2007 Dec; 8():82. PubMed ID: 18166138 [TBL] [Abstract][Full Text] [Related]
10. Functional analysis of novel RUNX2 mutations in cleidocranial dysplasia. Zeng L; Wei J; Han D; Liu H; Liu Y; Zhao N; Sun S; Wang Y; Feng H Mutagenesis; 2017 Jul; 32(4):437-443. PubMed ID: 28505335 [TBL] [Abstract][Full Text] [Related]
11. [Two novel RUNX2 gene mutations in two Chinese families with cleidocranial dysplasia]. Gao C; Wu L; Geng XJ; Song LJ; Luo Q Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):140-3. PubMed ID: 20376792 [TBL] [Abstract][Full Text] [Related]
12. The cleidocranial dysplasia-related R131G mutation in the Runt-related transcription factor RUNX2 disrupts binding to DNA but not CBF-beta. Han MS; Kim HJ; Wee HJ; Lim KE; Park NR; Bae SC; van Wijnen AJ; Stein JL; Lian JB; Stein GS; Choi JY J Cell Biochem; 2010 May; 110(1):97-103. PubMed ID: 20225274 [TBL] [Abstract][Full Text] [Related]
13. 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; 17(1):2. PubMed ID: 28056872 [TBL] [Abstract][Full Text] [Related]
14. [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; 48(11):834-8. PubMed ID: 21215027 [TBL] [Abstract][Full Text] [Related]
15. A novel single-base deletion mutation of the RUNX2 gene in a Chinese family with cleidocranial dysplasia. Fang CY; Xue JJ; Tan L; Jiang CH; Gao QP; Liang DS; Wu LQ Genet Mol Res; 2011 Dec; 10(4):3539-44. PubMed ID: 22194205 [TBL] [Abstract][Full Text] [Related]
16. A novel RUNX2 mutation (T420I) in Chinese patients with cleidocranial dysplasia. Wang GX; Sun RP; Song FL Genet Mol Res; 2010 Jan; 9(1):41-7. PubMed ID: 20082269 [TBL] [Abstract][Full Text] [Related]
17. A novel RUNX2 mutation in exon 8, G462X, in a patient with Cleidocranial Dysplasia. Jung YJ; Bae HS; Ryoo HM; Baek SH J Cell Biochem; 2018 Jan; 119(1):1152-1162. PubMed ID: 28703881 [TBL] [Abstract][Full Text] [Related]
18. Whole-exome sequencing of a novel initiation codon mutation in RUNX2 in a Chinese family with cleidocranial dysplasia. Yang L; Lu G; Shen W; Chen W; Lu H; Zhang G; Yuan S; Zheng S; Ren J Medicine (Baltimore); 2021 Nov; 100(45):e27746. PubMed ID: 34766588 [TBL] [Abstract][Full Text] [Related]
19. Familial cleidocranial dysplasia misdiagnosed as rickets over three generations. Franceschi R; Maines E; Fedrizzi M; Piemontese MR; De Bonis P; Agarwal N; Bellizzi M; Di Palma A Pediatr Int; 2015 Oct; 57(5):1003-6. PubMed ID: 26286462 [TBL] [Abstract][Full Text] [Related]
20. RUNX2 gene status in a cleidocranial dysplasia patient without supernumerary teeth. Anthonappa RP; King NM; Mahmoud Rabie AB J Investig Clin Dent; 2013 May; 4(2):124-7. PubMed ID: 23188595 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]