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 *

93 related articles for article (PubMed ID: 7258937)

  • 1. X-linked recessive ocular dystrophy with band keratopathy.
    Brenner M
    Ann Ophthalmol; 1981 Mar; 13(3):305-9. PubMed ID: 7258937
    [No Abstract]   [Full Text] [Related]  

  • 2. [Vitrectomy: method for treating of vitreo-corneal adhesions in children].
    Kazakbaev AG
    Vestn Oftalmol; 1998; 114(6):36-7. PubMed ID: 9951385
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Smith-Magenis syndrome.
    Finucane BM; Jaeger ER
    Ophthalmology; 1997 May; 104(5):732-3. PubMed ID: 9160013
    [No Abstract]   [Full Text] [Related]  

  • 4. Lowe's syndrome.
    Tripathi RC; Cibis GW; Harris DJ; Tripathi B
    Birth Defects Orig Artic Ser; 1982; 18(6):629-44. PubMed ID: 6890859
    [No Abstract]   [Full Text] [Related]  

  • 5. Genetic studies of congenital cataract.
    Mostafa MS; Temtamy S; El-Gammal MY; Sayed SI; Abdel-Salam M; El-Baroudy R
    Metab Pediatr Ophthalmol; 1981; 5(3-4):233-42. PubMed ID: 7311663
    [No Abstract]   [Full Text] [Related]  

  • 6. [Analysis of causes for penetrating keratoplasty at Shandong Eye Institute from 1997 to 2002].
    Xie LX; Wang FH; Shi WY
    Zhonghua Yan Ke Za Zhi; 2006 Aug; 42(8):704-8. PubMed ID: 17081441
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial intraocular cysts in association with anisometropia.
    Amer R; Anteby I
    Br J Ophthalmol; 2004 Oct; 88(10):1349-50. PubMed ID: 15377565
    [No Abstract]   [Full Text] [Related]  

  • 8. Brief clinical report: corneal dermoids and short stature in brother and sister--a new syndrome?
    Guízar-Vázquez J; Luengas-Muñoz FJ; Antillón F
    Am J Med Genet; 1981; 8(2):229-34. PubMed ID: 7282777
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new, X-linked endothelial corneal dystrophy.
    Schmid E; Lisch W; Philipp W; Lechner S; Göttinger W; Schlötzer-Schrehardt U; Müller T; Utermann G; Janecke AR
    Am J Ophthalmol; 2006 Mar; 141(3):478-487. PubMed ID: 16490493
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Analogy of Blaschko lines in the eye].
    Rott HD; Koniszewski G
    J Genet Hum; 1987 Jan; 35(1):19-27. PubMed ID: 3559520
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetics in pediatric ophthalmology.
    Bateman JB
    Pediatr Clin North Am; 1983 Dec; 30(6):1015-31. PubMed ID: 6359041
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multifactorial or polygenic inheritance in ophthalmology.
    François J
    Dev Ophthalmol; 1985; 10():1-39. PubMed ID: 3979643
    [No Abstract]   [Full Text] [Related]  

  • 13. [Keratotorus. Aetiology with regard to heredity (author's transl)].
    Eggers C
    Klin Monbl Augenheilkd; 1978 Oct; 173(4):551-7. PubMed ID: 732172
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bilateral Peter's anomaly in an infant with 49,XXXXY syndrome.
    Monaghan KG; Dennehy PJ; VanDyke DL; Weiss L
    J Pediatr Ophthalmol Strabismus; 1998; 35(2):112-3. PubMed ID: 9559511
    [No Abstract]   [Full Text] [Related]  

  • 15. Genetic counseling in congenital eye disorders.
    Bohár A; Czeizel A
    Ophthalmologica; 1983; 187(3):174-80. PubMed ID: 6415563
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A family with idiopathic recessive sex-linked retinoschisis].
    Guyot-Sionnest
    Ann Ocul (Paris); 1969 Jun; 202(6):573-98. PubMed ID: 5405757
    [No Abstract]   [Full Text] [Related]  

  • 17. A novel KERA mutation associated with autosomal recessive cornea plana.
    Khan A; Al-Saif A; Kambouris M
    Ophthalmic Genet; 2004 Jun; 25(2):147-52. PubMed ID: 15370545
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Vitreoretinochoroidal heredo-dystrophy, microcornea, glaucoma and cataract].
    François P; Puech B; Hache JC; Laffineur Q
    J Fr Ophtalmol; 1993; 16(1):29-40. PubMed ID: 8482797
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.
    Scheinman SJ; Pook MA; Wooding C; Pang JT; Frymoyer PA; Thakker RV
    J Clin Invest; 1993 Jun; 91(6):2351-7. PubMed ID: 8099916
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary mucoepithelial dysplasia, a disease of gap junction and desmosome formation.
    Witkop CJ; White JG; Waring GO
    Birth Defects Orig Artic Ser; 1982; 18(6):493-511. PubMed ID: 7171771
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.