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.
214 related articles for article (PubMed ID: 28971234)
1. A novel dominant COL11A1 mutation in a child with Stickler syndrome type II is associated with recurrent fractures. Vogiatzi MG; Li D; Tian L; Garifallou JP; Kim CE; Hakonarson H; Levine MA Osteoporos Int; 2018 Jan; 29(1):247-251. PubMed ID: 28971234 [TBL] [Abstract][Full Text] [Related]
2. Alternative splicing modifies the effect of mutations in COL11A1 and results in recessive type 2 Stickler syndrome with profound hearing loss. Richards AJ; Fincham GS; McNinch A; Hill D; Poulson AV; Castle B; Lees MM; Moore AT; Scott JD; Snead MP J Med Genet; 2013 Nov; 50(11):765-71. PubMed ID: 23922384 [TBL] [Abstract][Full Text] [Related]
3. A mild form of Stickler syndrome type II caused by mosaicism of COL11A1. Lauritsen KF; Lildballe DL; Coucke PJ; Monrad R; Larsen DA; Gregersen PA Eur J Med Genet; 2017 May; 60(5):275-278. PubMed ID: 28315471 [TBL] [Abstract][Full Text] [Related]
4. Variable clinical expression of Stickler Syndrome: A case report of a novel COL11A1 mutation. Brizola E; Gnoli M; Tremosini M; Nucci P; Bargiacchi S; La Barbera A; Giglio S; Sangiorgi L Mol Genet Genomic Med; 2020 Sep; 8(9):e1353. PubMed ID: 32558342 [TBL] [Abstract][Full Text] [Related]
5. Homozygous variants in AMPD2 and COL11A1 lead to a complex phenotype of pontocerebellar hypoplasia type 9 and Stickler syndrome type 2. Abreu NJ; Koboldt DC; Gastier-Foster JM; Dave-Wala A; Flanigan KM; Waldrop MA Am J Med Genet A; 2020 Mar; 182(3):557-560. PubMed ID: 31833174 [TBL] [Abstract][Full Text] [Related]
6. Mutation survey and genotype-phenotype analysis of COL2A1 and COL11A1 genes in 16 Chinese patients with Stickler syndrome. Wang X; Jia X; Xiao X; Li S; Li J; Li Y; Wei Y; Liang X; Guo X Mol Vis; 2016; 22():697-704. PubMed ID: 27390512 [TBL] [Abstract][Full Text] [Related]
7. Cephalometrics in Stickler syndrome: Objectification of the typical facial appearance. Acke FR; Dhooge IJ; Malfait F; De Leenheer EM; De Pauw GA J Craniomaxillofac Surg; 2016 Jul; 44(7):848-53. PubMed ID: 27193475 [TBL] [Abstract][Full Text] [Related]
8. Inherited and de novo biallelic pathogenic variants in COL11A1 result in type 2 Stickler syndrome with severe hearing loss. Nixon T; Richards AJ; Lomas A; Abbs S; Vasudevan P; McNinch A; Alexander P; Snead MP Mol Genet Genomic Med; 2020 Sep; 8(9):e1354. PubMed ID: 32578940 [TBL] [Abstract][Full Text] [Related]
9. Microphthalmia and congenital cataract in two patients with Stickler syndrome type II: a case report. Boysen KB; Tümer Z; Bach-Holm D; Bisgaard AM; Kessel L Ophthalmic Genet; 2024 Jun; 45(3):313-318. PubMed ID: 38299479 [TBL] [Abstract][Full Text] [Related]
10. A novel mutation in the COL2A1 gene in a patient with Stickler syndrome type 1: a case report and review of the literature. Higuchi Y; Hasegawa K; Yamashita M; Tanaka H; Tsukahara H J Med Case Rep; 2017 Aug; 11(1):237. PubMed ID: 28841907 [TBL] [Abstract][Full Text] [Related]
11. Deletions within COL11A1 in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA). Vijzelaar R; Waller S; Errami A; Donaldson A; Lourenco T; Rodrigues M; McConnell V; Fincham G; Snead M; Richards A BMC Med Genet; 2013 Apr; 14():48. PubMed ID: 23621912 [TBL] [Abstract][Full Text] [Related]
12. Novel pathogenic COL11A1/COL11A2 variants in Stickler syndrome detected by targeted NGS and exome sequencing. Acke FR; Malfait F; Vanakker OM; Steyaert W; De Leeneer K; Mortier G; Dhooge I; De Paepe A; De Leenheer EM; Coucke PJ Mol Genet Metab; 2014 Nov; 113(3):230-5. PubMed ID: 25240749 [TBL] [Abstract][Full Text] [Related]
13. Genetic testing results of children suspected to have Stickler syndrome type collagenopathy after ocular examination. Khan AO; AlAbdi L; Patel N; Helaby R; Hashem M; Abdulwahab F; AlBadr FB; Alkuraya FS Mol Genet Genomic Med; 2021 May; 9(5):e1628. PubMed ID: 33951325 [TBL] [Abstract][Full Text] [Related]
14. Phenotypic characterization of patients with early-onset high myopia due to mutations in Zhou L; Xiao X; Li S; Jia X; Wang P; Sun W; Zhang F; Li J; Li T; Zhang Q Mol Vis; 2018; 24():560-573. PubMed ID: 30181686 [TBL] [Abstract][Full Text] [Related]
16. Stickler syndrome and vitreoretinal degeneration: correlation between locus mutation and vitreous phenotype. Apropos of a case. Parentin F; Sangalli A; Mottes M; Perissutti P Graefes Arch Clin Exp Ophthalmol; 2001 Apr; 239(4):316-9. PubMed ID: 11450497 [TBL] [Abstract][Full Text] [Related]
17. Ocular complications and prophylactic strategies in Stickler syndrome: a systematic literature review. Boysen KB; La Cour M; Kessel L Ophthalmic Genet; 2020 Jun; 41(3):223-234. PubMed ID: 32316871 [TBL] [Abstract][Full Text] [Related]
18. Mutation Spectrum and De Novo Mutation Analysis in Stickler Syndrome Patients with High Myopia or Retinal Detachment. Huang L; Chen C; Wang Z; Sun L; Li S; Zhang T; Luo X; Ding X Genes (Basel); 2020 Aug; 11(8):. PubMed ID: 32756486 [TBL] [Abstract][Full Text] [Related]
19. Osteoporosis in Stickler syndrome. A new family case with bone histology study. Insalaco P; Legrand E; Bouvard B; Audran M Morphologie; 2017 Mar; 101(332):33-38. PubMed ID: 28159459 [TBL] [Abstract][Full Text] [Related]
20. Stickler syndrome: further mutations in COL11A1 and evidence for additional locus heterogeneity. Martin S; Richards AJ; Yates JR; Scott JD; Pope M; Snead MP Eur J Hum Genet; 1999; 7(7):807-14. PubMed ID: 10573014 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]