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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 3436724)

  • 21. 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]  

  • 22. Orthodontic treatment of a patient with Stickler syndrome.
    Suda N; Handa S; Higashihori N; Ogawa T; Tsuji M; Ohyama K
    Angle Orthod; 2007 Sep; 77(5):931-9. PubMed ID: 17902239
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations.
    Wubben TJ; Branham KH; Besirli CG; Bohnsack BL
    Ophthalmic Genet; 2018 Oct; 39(5):615-618. PubMed ID: 30130436
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Branchio-oto-renal syndrome.
    Millman B; Gibson WS; Foster WP
    Arch Otolaryngol Head Neck Surg; 1995 Aug; 121(8):922-5. PubMed ID: 7619422
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The Stickler syndrome (hereditary arthro-ophthalmopathy).
    Say B; Berry J; Barber N
    Clin Genet; 1977 Sep; 12(3):179-82. PubMed ID: 409578
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The hip in Stickler syndrome.
    Rose PS; Ahn NU; Levy HP; Magid D; Davis J; Liberfarb RM; Sponseller PD; Francomano CA
    J Pediatr Orthop; 2001; 21(5):657-63. PubMed ID: 11521037
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Ophthalmic and molecular genetic findings in Kniest dysplasia.
    Sergouniotis PI; Fincham GS; McNinch AM; Spickett C; Poulson AV; Richards AJ; Snead MP
    Eye (Lond); 2015 Apr; 29(4):475-82. PubMed ID: 25592122
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Craniofacial and extracranial malformations in the Klippel-Feil syndrome.
    Helmi C; Pruzansky S
    Cleft Palate J; 1980 Jan; 17(1):65-88. PubMed ID: 6928120
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Novel mutations in the COL2A1 gene in Japanese patients with Stickler syndrome.
    Kondo H; Matsushita I; Nagata T; Hayashi T; Kakinoki M; Uchio E; Kondo M; Ohji M; Kusaka S
    Hum Genome Var; 2016; 3():16018. PubMed ID: 27408751
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Dominantly inherited syndrome of microcephaly and cleft palate.
    Halal F
    Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Outcomes of surgery for retinal detachment in patients with Stickler syndrome: a comparison of two sequential 20-year cohorts.
    Abeysiri P; Bunce C; da Cruz L
    Graefes Arch Clin Exp Ophthalmol; 2007 Nov; 245(11):1633-8. PubMed ID: 17579881
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Thoracolumbar spinal abnormalities in Stickler syndrome.
    Rose PS; Ahn NU; Levy HP; Ahn UM; Davis J; Liberfarb RM; Nallamshetty L; Sponseller PD; Francomano CA
    Spine (Phila Pa 1976); 2001 Feb; 26(4):403-9. PubMed ID: 11224888
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient.
    Cerqueira DF; de Souza IP
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Mar; 105(3):353-7. PubMed ID: 18061493
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The Stickler syndrome presenting as a dominantly inherited cleft palate and blindness.
    Hall JG; Herrod H
    J Med Genet; 1975 Dec; 12(4):397-400. PubMed ID: 1219119
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Consideration of connective tissue dysfunction in the fragile X syndrome.
    Hagerman RJ; Van Housen K; Smith AC; McGavran L
    Am J Med Genet; 1984 Jan; 17(1):111-21. PubMed ID: 6711590
    [TBL] [Abstract][Full Text] [Related]  

  • 40. COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromes.
    Richards AJ; Martin S; Yates JR; Scott JD; Baguley DM; Pope FM; Snead MP
    Br J Ophthalmol; 2000 Apr; 84(4):364-71. PubMed ID: 10729292
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.