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.
225 related articles for article (PubMed ID: 12925722)
1. A glycine to aspartic acid substitution of COL2A1 in a family with the Strudwick variant of spondyloepimetaphyseal dysplasia. Tysoe C; Saunders J; White L; Hills N; Nicol M; Evans G; Cole T; Chapman S; Pope FM QJM; 2003 Sep; 96(9):663-71. PubMed ID: 12925722 [TBL] [Abstract][Full Text] [Related]
2. Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick type. Tiller GE; Polumbo PA; Weis MA; Bogaert R; Lachman RS; Cohn DH; Rimoin DL; Eyre DR Nat Genet; 1995 Sep; 11(1):87-9. PubMed ID: 7550321 [TBL] [Abstract][Full Text] [Related]
3. Dysspondyloenchondromatosis (DSC) associated with COL2A1 mutation: Clinical and radiological overlap with spondyloepimetaphyseal dysplasia-Strudwick type (SEMD-S). Merrick B; Calder A; Wakeling E Am J Med Genet A; 2015 Dec; 167A(12):3103-7. PubMed ID: 26250472 [TBL] [Abstract][Full Text] [Related]
4. Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: a case report. Chen J; Ma X; Zhou Y; Li G; Guo Q BMC Pediatr; 2017 Jul; 17(1):175. PubMed ID: 28738883 [TBL] [Abstract][Full Text] [Related]
5. COL2A1-related skeletal dysplasias with predominant metaphyseal involvement. Walter K; Tansek M; Tobias ES; Ikegawa S; Coucke P; Hyland J; Mortier G; Iwaya T; Nishimura G; Superti-Furga A; Unger S Am J Med Genet A; 2007 Jan; 143A(2):161-7. PubMed ID: 17163530 [TBL] [Abstract][Full Text] [Related]
6. A new form of severe spondyloepimetaphyseal dysplasia: clinical and radiological characterization. Isidor B; Geffroy L; de Courtivron B; Le Caignec C; Thiel CT; Mortier G; Cormier-Daire V; David A; Toutain A Am J Med Genet A; 2013 Oct; 161A(10):2645-51. PubMed ID: 23956136 [TBL] [Abstract][Full Text] [Related]
7. Phenotypic expressions of a Gly 154Arg mutation in type II collagen in two unrelated patients with spondyloepimetaphyseal dysplasia (SEMD). Kaitila I; Körkkö J; Marttinen E; Ala-Kokko L Am J Med Genet; 1996 May; 63(1):111-22. PubMed ID: 8723096 [TBL] [Abstract][Full Text] [Related]
8. A form of autosomal dominant spondyloepiphyseal dysplasia is caused by a glycine to alanine substitution in the COL2A1 gene. Sellick GS; Hoornaert KP; Mortier GR; King C; Dolling CL; Newbury-Ecob RA; Gargan M; Hall CM; Houlston RS; Smithson SF Clin Dysmorphol; 2006 Oct; 15(4):197-202. PubMed ID: 16957471 [TBL] [Abstract][Full Text] [Related]
9. Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies. Machol K; Jain M; Almannai M; Orand T; Lu JT; Tran A; Chen Y; Schlesinger A; Gibbs R; Bonafe L; Campos-Xavier AB; Unger S; Superti-Furga A; Lee BH; Campeau PM; Burrage LC Am J Med Genet A; 2017 Mar; 173(3):733-739. PubMed ID: 27888646 [TBL] [Abstract][Full Text] [Related]
11. Spondyloepiphyseal dysplasia congenita caused by double heterozygous mutations in COL2A1. Kawano O; Nakamura A; Morikawa S; Uetake K; Ishizu K; Tajima T Am J Med Genet A; 2015 Jul; 167(7):1578-81. PubMed ID: 25900302 [TBL] [Abstract][Full Text] [Related]
12. Mutation Update for COL2A1 Gene Variants Associated with Type II Collagenopathies. Barat-Houari M; Sarrabay G; Gatinois V; Fabre A; Dumont B; Genevieve D; Touitou I Hum Mutat; 2016 Jan; 37(1):7-15. PubMed ID: 26443184 [TBL] [Abstract][Full Text] [Related]
13. Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule. Richards AJ; Morgan J; Bearcroft PW; Pickering E; Owen MJ; Holmans P; Williams N; Tysoe C; Pope FM; Snead MP; Hughes H J Med Genet; 2002 Sep; 39(9):661-5. PubMed ID: 12205109 [TBL] [Abstract][Full Text] [Related]
14. Novel and recurrent COL2A1 mutations in Chinese patients with spondyloepiphyseal dysplasia. Cao LH; Wang L; Ji CY; Wang LB; Ma HW; Luo Y Genet Mol Res; 2012 Dec; 11(4):4130-7. PubMed ID: 23079993 [TBL] [Abstract][Full Text] [Related]
15. Low basal transcription of genes for tissue-specific collagens by fibroblasts and lymphoblastoid cells. Application to the characterization of a glycine 997 to serine substitution in alpha 1(II) collagen chains of a patient with spondyloepiphyseal dysplasia. Chan D; Cole WG J Biol Chem; 1991 Jul; 266(19):12487-94. PubMed ID: 1905723 [TBL] [Abstract][Full Text] [Related]
16. Substitution of aspartic acid for glycine at position 310 in type II collagen produces achondrogenesis II, and substitution of serine at position 805 produces hypochondrogenesis: analysis of genotype-phenotype relationships. Bonaventure J; Cohen-Solal L; Ritvaniemi P; Van Maldergem L; Kadhom N; Delezoide AL; Maroteaux P; Prockop DJ; Ala-Kokko L Biochem J; 1995 May; 307 ( Pt 3)(Pt 3):823-30. PubMed ID: 7741714 [TBL] [Abstract][Full Text] [Related]
17. A novel COL2A1 mutation causing spondyloepiphyseal dysplasia congenita in a Chinese family. Zhou T; Yang X; Chen Z; Zhou Y; Cao X; Zhao C; Zhao J J Clin Lab Anal; 2021 Apr; 35(4):e23728. PubMed ID: 33590889 [TBL] [Abstract][Full Text] [Related]
18. Novel amino acid substitution in the Y-position of collagen type II causes spondyloepimetaphyseal dysplasia congenita. Sulko J; Czarny-Ratajczak M; Wozniak A; Latos-Bielenska A; Kozlowski K Am J Med Genet A; 2005 Sep; 137A(3):292-7. PubMed ID: 16088915 [TBL] [Abstract][Full Text] [Related]
19. Association of a p.Pro786Leu variant in COL2A1 with mild spondyloepiphyseal dysplasia congenita in a three-generation family. Mark PR; Torres-Martinez W; Lachman RS; Weaver DD Am J Med Genet A; 2011 Jan; 155A(1):174-9. PubMed ID: 21204228 [TBL] [Abstract][Full Text] [Related]
20. Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneity. Gertner JM; Whyte MP; Dixon PH; Pang JT; Trump D; Pearce SH; Wooding C; Thakker RV J Bone Miner Res; 1997 Aug; 12(8):1204-9. PubMed ID: 9258750 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]