BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 4213352)

  • 1. Recent advances in ophthalmic genetics. Genetic counselling.
    Jay B
    Br J Ophthalmol; 1974 Apr; 58(4):427-37. PubMed ID: 4213352
    [No Abstract]   [Full Text] [Related]  

  • 2. Intermediate sex-linked inheritance.
    Blach RK; Jay B
    Br J Ophthalmol; 1969 Apr; 53(4):284-5. PubMed ID: 5781040
    [No Abstract]   [Full Text] [Related]  

  • 3. Genetics and counselling in ophthalmology.
    Keith CG
    Aust J Ophthalmol; 1981 Feb; 9(1):74-6. PubMed ID: 6793033
    [No Abstract]   [Full Text] [Related]  

  • 4. X-linked retinitis pigmentosa.
    Jay B; Bird A
    Trans Am Acad Ophthalmol Otolaryngol; 1973; 77(5):OP641-51. PubMed ID: 4784907
    [No Abstract]   [Full Text] [Related]  

  • 5. [Prenatal diagnosis of glycogenosis type II (Pompe) and subsequent therapeutic abortion (author's transl)].
    Schaub J; Osang M; von Bassewitz DB; Grote W; Terinde R; Lombeck I; Bremer HJ
    Dtsch Med Wochenschr; 1974 Nov; 99(44):2219-22, 27. PubMed ID: 4529697
    [No Abstract]   [Full Text] [Related]  

  • 6. X-linked recessive fundus dystrophies and their carrier states.
    Bird AC; Blach RK
    Trans Ophthalmol Soc U K (1962); 1970; 90():127-38. PubMed ID: 5283398
    [No Abstract]   [Full Text] [Related]  

  • 7. Enzyme therapy and prenatal diagnosis in glycogenosis type II.
    Hug G
    Am J Dis Child; 1974 Nov; 128(5):607-9. PubMed ID: 4278812
    [No Abstract]   [Full Text] [Related]  

  • 8. Sex-linked chorioretinal heredodegenerations.
    François J
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):99-116. PubMed ID: 4950918
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variable expression of albinism within a single kindred.
    Castronuovo S; Simon JW; Kandel GL; Morier A; Wolf B; Witkop CJ; Jenkins PL
    Am J Ophthalmol; 1991 Apr; 111(4):419-26. PubMed ID: 1901453
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe's disease).
    Koster JF; Slee RG; Hülsmann WC
    Clin Chim Acta; 1974 Mar; 51(3):319-25. PubMed ID: 4524047
    [No Abstract]   [Full Text] [Related]  

  • 11. Pompe's disease--detection of maternal heterozygote and antenatal exclusion in the fetus.
    Benson PF; Blunt S; Brown SP; Nash FW; Tiller M
    Guys Hosp Rep; 1972; 121(2):137-46. PubMed ID: 4269382
    [No Abstract]   [Full Text] [Related]  

  • 12. [Useful data in genetic counseling].
    François J
    Ann Ocul (Paris); 1972 Nov; 205(11):1173-80. PubMed ID: 4196608
    [No Abstract]   [Full Text] [Related]  

  • 13. Inherited eye diseases.
    Whitwell J
    Practitioner; 1975 May; 214(1283):621-630. PubMed ID: 1079941
    [No Abstract]   [Full Text] [Related]  

  • 14. Ocular manifestations in female carriers of X-linked disorders.
    Nowakowski R
    J Am Optom Assoc; 1995 Jun; 66(6):352-6. PubMed ID: 7673594
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X-linked ocular albinism: fundus of a heterozygous female.
    Costa DL; Huang SJ; Donsoff IM; Yannuzzi LA
    Retina; 2003 Jun; 23(3):410-1. PubMed ID: 12824848
    [No Abstract]   [Full Text] [Related]  

  • 16. [Choroideremia (progressive chorio-retinal degeneration)].
    François J; de Brabandere J; Stockmans L
    Bull Soc Belge Ophtalmol; 1967; 146():384-400. PubMed ID: 5311122
    [No Abstract]   [Full Text] [Related]  

  • 17. Retinal pigmentary disease.
    Podos SM
    Int Ophthalmol Clin; 1967; 7(4):935-48. PubMed ID: 5304605
    [No Abstract]   [Full Text] [Related]  

  • 18. Genetics in ophthalmology.
    Can J Ophthalmol; 1978 Jul; 13(3):135-7. PubMed ID: 698883
    [No Abstract]   [Full Text] [Related]  

  • 19. X-chromosomal-linked diseases affecting the eye: status of the heterozygote female.
    Krill AE
    Trans Am Ophthalmol Soc; 1969; 67():535-608. PubMed ID: 4985894
    [No Abstract]   [Full Text] [Related]  

  • 20. [Glycogenosis 3 - Pompe's disease - in a 1 1/2-month-old child].
    Papilova EI; Revenkova LA
    Pediatriia; 1975 May; (5):84-6. PubMed ID: 1056587
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.