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 *

145 related articles for article (PubMed ID: 7285774)

  • 21. A kindred showing a disorder of the retinal pigmentary epithelium and choriocapillaris, with characteristic macular changes and autosomal dominant transmission.
    Martyn LJ; Walker BA
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):189-92. PubMed ID: 5173141
    [No Abstract]   [Full Text] [Related]  

  • 22. Retinal dysplasia--A report of two surgical cases.
    Kaku T; Sasai K; Nagamine Y; Takahashi M
    Acta Pathol Jpn; 1975 May; 25(3):347-53. PubMed ID: 1155094
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel hereditary developmental vitreoretinopathy with multiple ocular abnormalities localizing to a 5-cM region of chromosome 5q13-q14.
    Black GC; Perveen R; Wiszniewski W; Dodd CL; Donnai D; McLeod D
    Ophthalmology; 1999 Nov; 106(11):2074-81. PubMed ID: 10571340
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Eye abnormalities associated with retinal dysplasia.
    Hunter WS
    Can J Ophthalmol; 1966 Jan; 1(1):52-5. PubMed ID: 4958169
    [No Abstract]   [Full Text] [Related]  

  • 25. Chorio-retinal dysplasia, microcephaly and mental retardation. An autosomal dominant syndrome.
    Tenconi R; Clementi M; Moschini GB; Casara G; Baccichetti C
    Clin Genet; 1981 Nov; 20(5):347-51. PubMed ID: 7333029
    [No Abstract]   [Full Text] [Related]  

  • 26. Dorsal retinal pigment epithelium differentiates as neural retina in the microphthalmia (mi/mi) mouse.
    Bumsted KM; Barnstable CJ
    Invest Ophthalmol Vis Sci; 2000 Mar; 41(3):903-8. PubMed ID: 10711712
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Meridional folds, meridional complexes, and associated abnormalities of the peripheral retina.
    Spencer LM; Foos RY; Straatsma BR
    Am J Ophthalmol; 1970 Nov; 70(5):679-714. PubMed ID: 5477154
    [No Abstract]   [Full Text] [Related]  

  • 28. Fundus findings in a case of Joubert syndrome.
    Chawla R; Bypareddy R; Vekaria L; Venkatesh P; Ananthashayana VH
    Indian J Ophthalmol; 2017 Apr; 65(4):329-330. PubMed ID: 28513504
    [No Abstract]   [Full Text] [Related]  

  • 29. Primary retinal dysplasia transmitted as X-chromosome-linked recessive disorder.
    Godel V; Romano A; Stein R; Adam A; Goodman RM
    Am J Ophthalmol; 1978 Aug; 86(2):221-7. PubMed ID: 567435
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Sectoral iris heterochromia and retinal pigment variation in 13q-syndrome.
    Kutzbach B; Mendelsohn N; Rath P; Summers CG
    J AAPOS; 2007 Oct; 11(5):513-5. PubMed ID: 17933676
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Ocular malformations and lissencephaly.
    Warburg M
    Eur J Pediatr; 1987 Sep; 146(5):450-2. PubMed ID: 3119342
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Heterotopic ciliary epithelial differentiation in a patient with trisomy 13.
    Michon JJ; Borges JM; Tso MO
    J Pediatr Ophthalmol Strabismus; 1991; 28(1):23-7. PubMed ID: 2019954
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Retinal dysplasia. Morphological identity of the retinal dysplasia syndrome (Reese) and D (13-15) trisomy syndrome (Patau)].
    Iwig M
    Zentralbl Allg Pathol; 1969; 112(5):492-504. PubMed ID: 5198066
    [No Abstract]   [Full Text] [Related]  

  • 34. Congenital blindness with ocular developmental anomalies, including retinal dysplasia, in Doberman Pinscher dogs.
    Bergsjø T; Arnesen K; Heim P; Nes N
    J Am Vet Med Assoc; 1984 Jun; 184(11):1383-6. PubMed ID: 6429110
    [TBL] [Abstract][Full Text] [Related]  

  • 35. RPE dysplasia with retinal duplication in a mutant mouse strain.
    Cook CS; Generoso WM; Hester D; Peiffer RL
    Exp Eye Res; 1991 Apr; 52(4):409-15. PubMed ID: 2037019
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Retinal dysplasia].
    Koronczewska D
    Klin Oczna; 1974 Jun; 44(6):601-3. PubMed ID: 4849645
    [No Abstract]   [Full Text] [Related]  

  • 37. Index of suspicion. Case 2. Diagnosis: Norrie disease.
    Veeramachaneni VV; Fielder PN
    Pediatr Rev; 2001 Jun; 22(6):211-5. PubMed ID: 11436222
    [No Abstract]   [Full Text] [Related]  

  • 38. Defects in retinal pigment epithelium cell proliferation and retinal attachment in mutant mice with p27(Kip1) gene ablation.
    Defoe DM; Adams LB; Sun J; Wisecarver SN; Levine EM
    Mol Vis; 2007 Feb; 13():273-86. PubMed ID: 17356514
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Retinal pigment epithelium in incontinentia pigmenti.
    Mensheha-Manhart O; Rodrigues MM; Shields JA; Shannon GM; Mirabelli RP
    Am J Ophthalmol; 1975 Apr; 79(4):571-7. PubMed ID: 1119517
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Glioneuroma associated with colobomatous dysplasia of the anterior uvea and retina. A case simulating medulloepithelioma.
    Kivelä T; Kauniskangas L; Miettinen P; Tarkkanen A
    Ophthalmology; 1989 Dec; 96(12):1799-808. PubMed ID: 2622623
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.