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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

174 related items for PubMed ID: 4192495

  • 1. Hereditary blindness among Pingelapese people of Eastern Caroline Islands.
    Brody JA, Hussels I, Brink E, Torres J.
    Lancet; 1970 Jun 13; 1(7659):1253-7. PubMed ID: 4192495
    [No Abstract] [Full Text] [Related]

  • 2. [Causes of blindness in Tunisian children].
    Ayed S, Daghfous F, Guermazi K, Ben Osman N.
    Rev Int Trach Pathol Ocul Trop Subtrop Sante Publique; 1991 Jun 13; 68():123-8. PubMed ID: 1669642
    [Abstract] [Full Text] [Related]

  • 3. Pingelap and Mokil Atolls: achromatopsia.
    Hussels IE, Morton NE.
    Am J Hum Genet; 1972 May 13; 24(3):304-9. PubMed ID: 4555088
    [No Abstract] [Full Text] [Related]

  • 4. Homozygosity mapping of the Achromatopsia locus in the Pingelapese.
    Winick JD, Blundell ML, Galke BL, Salam AA, Leal SM, Karayiorgou M.
    Am J Hum Genet; 1999 Jun 13; 64(6):1679-85. PubMed ID: 10330355
    [Abstract] [Full Text] [Related]

  • 5. Rod Monochromatism (Achromatopsia).
    Tsang SH, Sharma T.
    Adv Exp Med Biol; 2018 Jun 13; 1085():119-123. PubMed ID: 30578497
    [Abstract] [Full Text] [Related]

  • 6. Achromatopsia in Pingelap Islanders. Study of a genetic isolate.
    Carr RE, Morton NE, Siegel IM.
    Am J Ophthalmol; 1971 Oct 13; 72(4):746-56. PubMed ID: 5315519
    [No Abstract] [Full Text] [Related]

  • 7. [Typical monochromacy, congenital deafness, and resistance to intracellular action of thyroid hormone (author's transl)].
    Newell FW, Diddie KR.
    Klin Monbl Augenheilkd; 1977 Nov 13; 171(5):731-4. PubMed ID: 304503
    [Abstract] [Full Text] [Related]

  • 8. Incomplete achromatopsia: diagnosis in infancy.
    Keith CG.
    Birth Defects Orig Artic Ser; 1982 Nov 13; 18(6):269-80. PubMed ID: 6983369
    [No Abstract] [Full Text] [Related]

  • 9. Prevalence and causes of blindness in urban and rural areas of Egypt.
    Said ME, Goldstein H, Korra A, El-Kashlan K.
    Public Health Rep (1896); 1970 Jul 13; 85(7):587-99. PubMed ID: 4987473
    [No Abstract] [Full Text] [Related]

  • 10. [Etiology of blindness in Chad].
    Vedy J.
    Med Trop (Mars); 1972 Jul 13; 32():Suppl:427-33. PubMed ID: 4641951
    [No Abstract] [Full Text] [Related]

  • 11. New data on the vision of South American Indians.
    Salzano FM, Neel JV.
    Bull Pan Am Health Organ; 1976 Jul 13; 10(1):1-7. PubMed ID: 1084771
    [Abstract] [Full Text] [Related]

  • 12. Genes and colour blindness.
    Lancet; 1990 Feb 03; 335(8684):263-4. PubMed ID: 1967724
    [No Abstract] [Full Text] [Related]

  • 13. Sorsby's familial pseudo-inflammatory macular dystrophy.
    Fraser HB, Wallace DC.
    Am J Ophthalmol; 1971 Jun 03; 71(6):1216-20. PubMed ID: 5314577
    [No Abstract] [Full Text] [Related]

  • 14. [Hereditary macular degenerations].
    François J.
    Ophthalmologica; 1974 Jun 03; 168(6):417-45. PubMed ID: 4603577
    [No Abstract] [Full Text] [Related]

  • 15. A locus for autosomal recessive achromatopsia on human chromosome 8q.
    Milunsky A, Huang XL, Milunsky J, DeStefano A, Baldwin CT.
    Clin Genet; 1999 Jul 03; 56(1):82-5. PubMed ID: 10466422
    [Abstract] [Full Text] [Related]

  • 16. Progressive cone dystrophy associated with mutation in CNGB3.
    Michaelides M, Aligianis IA, Ainsworth JR, Good P, Mollon JD, Maher ER, Moore AT, Hunt DM.
    Invest Ophthalmol Vis Sci; 2004 Jun 03; 45(6):1975-82. PubMed ID: 15161866
    [Abstract] [Full Text] [Related]

  • 17. Progressive generalized cone dysfunction.
    François J, de Rouck A, Verriest G, de Laey JJ, Cambie E.
    Ophthalmologica; 1974 Jun 03; 169(4):255-84. PubMed ID: 4547582
    [No Abstract] [Full Text] [Related]

  • 18. Cone dystrophy with dominant inheritance.
    Pearlman JT, Owen WG, Brounley DW, Sheppard JJ.
    Am J Ophthalmol; 1974 Mar 03; 77(3):293-303. PubMed ID: 4544306
    [No Abstract] [Full Text] [Related]

  • 19. Snowflake degeneration in hereditary vitreoretinal degeneration.
    Hirose T, Lee KY, Schepens CL.
    Am J Ophthalmol; 1974 Feb 03; 77(2):143-53. PubMed ID: 4812083
    [No Abstract] [Full Text] [Related]

  • 20. [Heredity of congenital deficiencies in color vision].
    François J, De Bie S, Verriest G, Matton MT.
    Acta Genet Med Gemellol (Roma); 1972 Jul 03; 21(3):233-56. PubMed ID: 4592447
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.