BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 1536174)

  • 1. 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]  

  • 2. [Vitreoretinal changes in siblings of two patients with Stickler syndrome. Study of two families].
    Langmann A; Langmann G; Kainer U; Faulborn J
    Ophthalmologe; 1993 Oct; 90(5):506-9. PubMed ID: 8219641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [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]  

  • 5. A dominantly inherited syndrome of hyaloideoretinal degeneration, cleft palate and maxillary hypoplasia (Cervenka syndrome).
    Cohen MM; Knobloch WH; Gorlin RJ
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):83-6. PubMed ID: 5173248
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Correlation of linkage data with phenotype in eight families with Stickler syndrome.
    Wilkin DJ; Mortier GR; Johnson CL; Jones MC; de Paepe A; Shohat M; Wildin RS; Falk RE; Cohn DH
    Am J Med Genet; 1998 Nov; 80(2):121-7. PubMed ID: 9805127
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary arthro-ophthalmopathy (the Stickler syndrome). Report of a kindred with protrusio acetabuli.
    Beals RK
    Clin Orthop Relat Res; 1977 Jun; (125):32-5. PubMed ID: 880775
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Stickler syndrome: an underdiagnosed disease. Report of a family.
    De Keyzer TH; De Veuster I; Smets RM
    Bull Soc Belge Ophtalmol; 2011; (318):45-9. PubMed ID: 22003765
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic and clinical heterogeneity of Stickler syndrome.
    Vintiner GM; Temple IK; Middleton-Price HR; Baraitser M; Malcolm S
    Am J Med Genet; 1991 Oct; 41(1):44-8. PubMed ID: 1683158
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Osteochondritis dissecans of the knee in an adult with Stickler syndrome.
    Trepman E
    Orthop Rev; 1993 Mar; 22(3):371-6. PubMed ID: 8474775
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The arthropathy of hereditary arthroophthalmopathy (Stickler syndrome).
    Lewkonia RM
    J Rheumatol; 1992 Aug; 19(8):1271-5. PubMed ID: 1404165
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. What all nurses need to know about Stickler syndrome.
    Brown E; Brown J; Hughes W; Marland GR
    Nurs Times; 2003 Apr 1-7; 99(13):28-9. PubMed ID: 12715553
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Stickler-like syndrome due to a dominant negative mutation in the COL2A1 gene.
    Ballo R; Beighton PH; Ramesar RS
    Am J Med Genet; 1998 Oct; 80(1):6-11. PubMed ID: 9800905
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Polyvalvular heart disease with joint hypermobility, characteristic facies, and particular skin abnormalities: new cases of "polyvalvular heart disease syndrome" or new association?
    Edouard T; Prost-Squarcioni C; Dulac Y; Vaysse F; Cavé H; Saugier-Veber P; Bourrouillou G; Verloes A; Tauber M; Bieth E
    Eur J Med Genet; 2010; 53(1):29-34. PubMed ID: 19932204
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular diagnosis of Stickler syndrome: a COL2A1 stop codon mutation screening strategy that is not compromised by mutant mRNA instability.
    Freddi S; Savarirayan R; Bateman JF
    Am J Med Genet; 2000 Feb; 90(5):398-406. PubMed ID: 10706362
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.