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.
145 related articles for article (PubMed ID: 18950500)
1. Significant ophthalmoarthropathy associated with ectodermal dysplasia in a child with Marshall-Stickler overlap: a case report. Al Kaissi A; Ganger R; Klaushofer K; Grill F Cases J; 2008 Oct; 1(1):270. PubMed ID: 18950500 [TBL] [Abstract][Full Text] [Related]
2. The Marshall syndrome: report of a new family and review of the literature. Shanske AL; Bogdanow A; Shprintzen RJ; Marion RW Am J Med Genet; 1997 May; 70(1):52-7. PubMed ID: 9129742 [TBL] [Abstract][Full Text] [Related]
3. A case with oto-spondylo-mega-epiphyseal-dysplasia (OSMED): the clinical recognition and differential diagnosis. Karaer K; Rosti RO; Torun D; Sanal HT; Bahçe M; Güran S Turk J Pediatr; 2011; 53(3):346-51. PubMed ID: 21980822 [TBL] [Abstract][Full Text] [Related]
4. Importance of early diagnosis of Stickler syndrome in newborns. Antunes RB; Alonso N; Paula RG J Plast Reconstr Aesthet Surg; 2012 Aug; 65(8):1029-34. PubMed ID: 22424767 [TBL] [Abstract][Full Text] [Related]
5. Visual complications of Stickler syndrome in paediatric patients with Robin sequence. Huang F; Kuo HK; Hsieh CH; Lai JP; Chen PK J Craniomaxillofac Surg; 2007 Mar; 35(2):76-80. PubMed ID: 17442580 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. The Weissenbacher-Zweymüller syndrome: possible neonatal expression of the Stickler syndrome. Kelly TE; Wells HH; Tuck KB Am J Med Genet; 1982 Jan; 11(1):113-9. PubMed ID: 7064999 [TBL] [Abstract][Full Text] [Related]
8. Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia. Chemke J; Carmi R; Galil A; Bar-Ziv Y; Ben-Ytzhak I; Zurkowski L Am J Med Genet; 1992 Aug; 43(6):989-95. PubMed ID: 1415350 [TBL] [Abstract][Full Text] [Related]
9. Stickler syndrome in Pierre-Robin sequence prenatal ultrasonographic diagnosis and postnatal therapy: two cases report. Pacella E; Malvasi A; Tinelli A; Laterza F; Dell'Edera D; Pacella F; Mazzeo F; Ferraresi A; Malarska KG; Cavallotti C Eur Rev Med Pharmacol Sci; 2010 Dec; 14(12):1051-4. PubMed ID: 21375138 [TBL] [Abstract][Full Text] [Related]
10. The Weissenbacher-Zweymüller, Stickler, and Marshall syndromes: further evidence for their identity. Winter RM; Baraitser M; Laurence KM; Donnai D; Hall CM Am J Med Genet; 1983 Oct; 16(2):189-99. PubMed ID: 6650564 [TBL] [Abstract][Full Text] [Related]
11. Marshall and stickler syndrome in one family. Tomčíková D; Bušányová B; Krásnik V; Gerinec A Cesk Slov Oftalmol; 2018; 74(3):108-111. PubMed ID: 30650974 [TBL] [Abstract][Full Text] [Related]
12. Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes. Annunen S; Körkkö J; Czarny M; Warman ML; Brunner HG; Kääriäinen H; Mulliken JB; Tranebjaerg L; Brooks DG; Cox GF; Cruysberg JR; Curtis MA; Davenport SL; Friedrich CA; Kaitila I; Krawczynski MR; Latos-Bielenska A; Mukai S; Olsen BR; Shinno N; Somer M; Vikkula M; Zlotogora J; Prockop DJ; Ala-Kokko L Am J Hum Genet; 1999 Oct; 65(4):974-83. PubMed ID: 10486316 [TBL] [Abstract][Full Text] [Related]
13. [Lens coloboma and lens dislocation in Stickler (Marshall) syndrome]. Schlote T; Völker M; Knorr M; Thiel HJ Klin Monbl Augenheilkd; 1997 Apr; 210(4):227-8. PubMed ID: 9235398 [TBL] [Abstract][Full Text] [Related]
14. Marshall syndrome: further evidence of a distinct phenotypic entity and report of new findings. Khalifa O; Imtiaz F; Ramzan K; Allam R; Hemidan AA; Faqeih E; Abuharb G; Balobaid A; Sakati N; Owain MA Am J Med Genet A; 2014 Oct; 164A(10):2601-6. PubMed ID: 25073711 [TBL] [Abstract][Full Text] [Related]
15. Clinical and Molecular genetics of Stickler syndrome. Snead MP; Yates JR J Med Genet; 1999 May; 36(5):353-9. PubMed ID: 10353778 [TBL] [Abstract][Full Text] [Related]
16. [Marshall syndrome: Clinical, radiological and genetical features of a Tunisian family]. Sakka R; Kerkeni E; Chaabouni M; Chioukh FZ; Ben Amor S; M'rad R; Ben Yahia S; Chaabouni H; Monastiri K Tunis Med; 2015 Mar; 93(3):170-4. PubMed ID: 26367406 [TBL] [Abstract][Full Text] [Related]
17. The Stickler syndrome: case reports and literature review. Bowling EL; Brown MD; Trundle TV Optometry; 2000 Mar; 71(3):177-82. PubMed ID: 10970261 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Diffuse Palmoplantar Keratoderma, Onychodystrophy, universal Hypotrichosis and Cysts. Arif T; Amin SS; Adil M; Mohtashim M Acta Dermatovenerol Croat; 2017 Jul; 25(2):161-163. PubMed ID: 28871934 [TBL] [Abstract][Full Text] [Related]