146 related articles for article (PubMed ID: 12511844)
21. Feeding Difficulty in an Infant with Stickler's Syndrome.
Vijay P; Kumaran P; Xavier AM; Varma RB; Kumar JS
Contemp Clin Dent; 2019; 10(3):558-560. PubMed ID: 32308337
[TBL] [Abstract][Full Text] [Related]
22. Congenital myopia in Stickler's hereditary arthro-ophthalmopathy.
Wang FM; Afran SI; Goldberg RB
Am J Ophthalmol; 1990 Oct; 110(4):435-6. PubMed ID: 2220987
[No Abstract] [Full Text] [Related]
23. Hereditary progressive arthro-ophthalmopathy of Stickler.
Blair NP; Albert DM; Liberfarb RM; Hirose T
Am J Ophthalmol; 1979 Nov; 88(5):876-88. PubMed ID: 507166
[TBL] [Abstract][Full Text] [Related]
24. Early-onset progressive osteoarthritis with hereditary progressive ophtalmopathy or Stickler syndrome.
Couchouron T; Masson C
Joint Bone Spine; 2011 Jan; 78(1):45-9. PubMed ID: 20462780
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Camptodactyly, polyepiphyseal dysplasia and mixed crystal deposition disease.
Hamza M; Bardin T
J Rheumatol; 1989 Aug; 16(8):1153-8. PubMed ID: 2585415
[TBL] [Abstract][Full Text] [Related]
27. [Stickler's syndrome (dystrophia vitreoretinalis hereditaria). Results of surgery for retinal detachment].
Karel I; Dolezalová J; Oudová P
Cesk Slov Oftalmol; 2001 May; 57(3):147-54. PubMed ID: 11433587
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. [Stickler's syndrome: case report with intrafamilial variability].
Groebe H; Pfeiffer RA
J Genet Hum; 1976 Nov; 24 Suppl():249-52. PubMed ID: 1025277
[No Abstract] [Full Text] [Related]
30. The Wagner-Stickler syndrome: a study of 22 families.
Liberfarb RM; Hirose T; Holmes LB
J Pediatr; 1981 Sep; 99(3):394-9. PubMed ID: 7264793
[TBL] [Abstract][Full Text] [Related]
31. Stickler syndrome. Presenting as a syndrome of cleft palate, myopia and blindness inherited as a dominant trait.
Hall J
Birth Defects Orig Artic Ser; 1974; 10(8):157-71. PubMed ID: 4218495
[No Abstract] [Full Text] [Related]
32. [Genetic and ophthalmological assessment of patients with type II Stickler syndrome].
Dias VG; Salem MC; Benetti Filho CC
Arq Bras Oftalmol; 2006; 69(6):881-7. PubMed ID: 17273684
[TBL] [Abstract][Full Text] [Related]
33. The diagnosis and consequences of Stickler syndrome.
Webb AC; Markus AF
Br J Oral Maxillofac Surg; 2002 Feb; 40(1):49-51. PubMed ID: 11883970
[TBL] [Abstract][Full Text] [Related]
34. A phenotypic variant of Knobloch syndrome.
Williams TA; Kirkby GR; Williams D; Ainsworth JR
Ophthalmic Genet; 2008 Jun; 29(2):85-6. PubMed ID: 18484314
[TBL] [Abstract][Full Text] [Related]
35. A-2-->G transition at the 3' acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindred.
Williams CJ; Ganguly A; Considine E; McCarron S; Prockop DJ; Walsh-Vockley C; Michels VV
Am J Med Genet; 1996 Jun; 63(3):461-7. PubMed ID: 8737653
[TBL] [Abstract][Full Text] [Related]
36. Variability of Stickler syndrome.
Zlotogora J; Sagi M; Schuper A; Leiba H; Merin S
Am J Med Genet; 1992 Feb; 42(3):337-9. PubMed ID: 1536174
[TBL] [Abstract][Full Text] [Related]
37. [Stickler's syndrome].
Goś R; Krawczykowa Z; Trzciński J
Klin Oczna; 1992 Jan; 94(1):32-3. PubMed ID: 1635370
[TBL] [Abstract][Full Text] [Related]
38. Stickler's syndrome associated with congenital glaucoma.
Ziakas NG; Ramsay AS; Lynch SA; Clarke MP
Ophthalmic Genet; 1998 Mar; 19(1):55-8. PubMed ID: 9587930
[TBL] [Abstract][Full Text] [Related]
39. Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene.
Bonaventure J; Philippe C; Plessis G; Vigneron J; Lasselin C; Maroteaux P; Gilgenkrantz S
Hum Genet; 1992; 90(1-2):164-8. PubMed ID: 1358786
[TBL] [Abstract][Full Text] [Related]
40. Clinical description and exclusion of candidate genes in a novel autosomal recessively inherited vitreoretinal dystrophy.
Sarra GM; Weigell-Weber M; Kotzot D; Niemeyer G; Messmer E; Hergersberg M
Arch Ophthalmol; 2003 Aug; 121(8):1109-16. PubMed ID: 12912687
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
