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2. Alternative splicing of exon 12 of the COL2A1 gene interrupts the triple helix of type-II collagen in the Kniest form of spondyloepiphyseal dysplasia. Chen L; Yang W; Cole WG J Orthop Res; 1996 Sep; 14(5):712-21. PubMed ID: 8893763 [TBL] [Abstract][Full Text] [Related]
3. The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene. Hoornaert KP; Dewinter C; Vereecke I; Beemer FA; Courtens W; Fryer A; Fryssira H; Lees M; Müllner-Eidenböck A; Rimoin DL; Siderius L; Superti-Furga A; Temple K; Willems PJ; Zankl A; Zweier C; De Paepe A; Coucke P; Mortier GR J Med Genet; 2006 May; 43(5):406-13. PubMed ID: 16155195 [TBL] [Abstract][Full Text] [Related]
4. Alport syndrome. Molecular genetic aspects. Hertz JM Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970 [TBL] [Abstract][Full Text] [Related]
5. High efficiency of mutation detection in type 1 stickler syndrome using a two-stage approach: vitreoretinal assessment coupled with exon sequencing for screening COL2A1. Richards AJ; Laidlaw M; Whittaker J; Treacy B; Rai H; Bearcroft P; Baguley DM; Poulson A; Ang A; Scott JD; Snead MP Hum Mutat; 2006 Jul; 27(7):696-704. PubMed ID: 16752401 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Clinical evaluation and COL2A1 gene analysis in 21 Brazilian families with Stickler syndrome: identification of novel mutations, further genotype/phenotype correlation, and its implications for the diagnosis. Zechi-Ceide RM; Jesus Oliveira NA; Guion-Almeida ML; Antunes LF; Richieri-Costa A; Passos-Bueno MR Eur J Med Genet; 2008; 51(3):183-96. PubMed ID: 18276201 [TBL] [Abstract][Full Text] [Related]
8. Missense and nonsense mutations in the alternatively-spliced exon 2 of COL2A1 cause the ocular variant of Stickler syndrome. McAlinden A; Majava M; Bishop PN; Perveen R; Black GC; Pierpont ME; Ala-Kokko L; Männikkö M Hum Mutat; 2008 Jan; 29(1):83-90. PubMed ID: 17721977 [TBL] [Abstract][Full Text] [Related]
9. Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect. Winterpacht A; Hilbert M; Schwarze U; Mundlos S; Spranger J; Zabel BU Nat Genet; 1993 Apr; 3(4):323-6. PubMed ID: 7981752 [TBL] [Abstract][Full Text] [Related]
10. Dominant negative mutations in the C-propeptide of COL2A1 cause platyspondylic lethal skeletal dysplasia, torrance type, and define a novel subfamily within the type 2 collagenopathies. Zankl A; Neumann L; Ignatius J; Nikkels P; Schrander-Stumpel C; Mortier G; Omran H; Wright M; Hilbert K; Bonafé L; Spranger J; Zabel B; Superti-Furga A Am J Med Genet A; 2005 Feb; 133A(1):61-7. PubMed ID: 15643621 [TBL] [Abstract][Full Text] [Related]
11. Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1. Richards AJ; McNinch A; Martin H; Oakhill K; Rai H; Waller S; Treacy B; Whittaker J; Meredith S; Poulson A; Snead MP Hum Mutat; 2010 Jun; 31(6):E1461-71. PubMed ID: 20513134 [TBL] [Abstract][Full Text] [Related]
12. A novel mutation of COL2A1 resulting in dominantly inherited rhegmatogenous retinal detachment. Richards AJ; Meredith S; Poulson A; Bearcroft P; Crossland G; Baguley DM; Scott JD; Snead MP Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):663-8. PubMed ID: 15671297 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. A mouse model for Stickler's syndrome: ocular phenotype of mice carrying a targeted heterozygous inactivation of type II (pro)collagen gene (Col2a1). Kaarniranta K; Ihanamäki T; Sahlman J; Pulkkinen H; Uusitalo H; Arita M; Tammi R; Lammi MJ; Helminen HJ Exp Eye Res; 2006 Aug; 83(2):297-303. PubMed ID: 16546167 [TBL] [Abstract][Full Text] [Related]
16. Autosomal dominant spondylarthropathy due to a type II procollagen gene (COL2A1) point mutation. Winterpacht A; Hilbert M; Schwarze U; Mundlos S; Spranger J; Zabel B Hum Mutat; 1994; 4(4):257-62. PubMed ID: 7866404 [TBL] [Abstract][Full Text] [Related]
17. The expanding spectrum of COL2A1 gene variants IN 136 patients with a skeletal dysplasia phenotype. Barat-Houari M; Dumont B; Fabre A; Them FT; Alembik Y; Alessandri JL; Amiel J; Audebert S; Baumann-Morel C; Blanchet P; Bieth E; Brechard M; Busa T; Calvas P; Capri Y; Cartault F; Chassaing N; Ciorca V; Coubes C; David A; Delezoide AL; Dupin-Deguine D; El Chehadeh S; Faivre L; Giuliano F; Goldenberg A; Isidor B; Jacquemont ML; Julia S; Kaplan J; Lacombe D; Lebrun M; Marlin S; Martin-Coignard D; Martinovic J; Masurel A; Melki J; Mozelle-Nivoix M; Nguyen K; Odent S; Philip N; Pinson L; Plessis G; Quélin C; Shaeffer E; Sigaudy S; Thauvin C; Till M; Touraine R; Vigneron J; Baujat G; Cormier-Daire V; Le Merrer M; Geneviève D; Touitou I Eur J Hum Genet; 2016 Jul; 24(7):992-1000. PubMed ID: 26626311 [TBL] [Abstract][Full Text] [Related]
18. Occurrence of deletion of a COL2A1 allele as the mutation in Stickler syndrome shows that a collagen type II dosage effect underlies this syndrome. Van Der Hout AH; Verlind E; Beemer FA; Buys CH; Hofstra RM; Scheffer H Hum Mutat; 2002 Sep; 20(3):236. PubMed ID: 12204008 [TBL] [Abstract][Full Text] [Related]
19. Stickler and branchio-oto-renal syndromes in a patient with mutations in EYA1 and COL2A1 genes. Olavarrieta L; Morales-Angulo C; del Castillo I; Moreno F; Moreno-Pelayo MA Clin Genet; 2008 Mar; 73(3):262-7. PubMed ID: 18177466 [TBL] [Abstract][Full Text] [Related]
20. A Heterozygous Mutation in the Triple Helical Region of the Alpha 1 (II) Chain of the COL2A1 Protein Causes Non-Lethal Spondyloepiphyseal Dysplasia Congenita. Almatrafi A; Alfadhli F; Khan YN; Afzal S; Hashmi JA; Ullah A; Albalawi AM; Basit S Genet Test Mol Biomarkers; 2019 May; 23(5):310-315. PubMed ID: 30932712 [No Abstract] [Full Text] [Related] [Next] [New Search]