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Journal Abstract Search

64 related items for PubMed ID: 1079303

  • 1. Letter: Genetically inherited traits in an Amish population.
    Fogland WG.
    Med J Aust; 1975 Feb 22; 1(8):253-4. PubMed ID: 1079303
    [No Abstract] [Full Text] [Related]

  • 2. Molecular genetics of infantile-onset retinal dystrophies.
    Moradi P, Moore AT.
    Eye (Lond); 2007 Oct 22; 21(10):1344-51. PubMed ID: 17914438
    [Abstract] [Full Text] [Related]

  • 3. [Inborn micro-errors in the retinal metabolism. Dichromasy,Oguchi's disease and other heredititary functional disorders of the retina].
    ten Doesschate J.
    Ned Tijdschr Geneeskd; 1967 Oct 07; 111(40):1737-9. PubMed ID: 5299835
    [No Abstract] [Full Text] [Related]

  • 4. Genetic studies in some ethnic groups of Pakistan (Southern Punjab): colour blindness, ear lobe attachment and behavioural traits.
    Mian A, Bhutta AM, Mushtaq R.
    Anthropol Anz; 1994 Mar 07; 52(1):17-22. PubMed ID: 8192432
    [Abstract] [Full Text] [Related]

  • 5. Description of Amish Study data set.
    Egeland JA, Gerhard DS, Pauls DL.
    Genet Epidemiol; 1989 Mar 07; 6(1):195-9. PubMed ID: 2786484
    [Abstract] [Full Text] [Related]

  • 6. Genetic studies of Pangwalas, Transhumant and Settled Gaddis. 4. Colour blindness, mid-phalangeal hair, ear lobe attachment and behavioural traits.
    Bhasin MK, Singh IP, Walter H, Bhasin V, Chahal SM, Singh R.
    Anthropol Anz; 1986 Mar 07; 44(1):45-53. PubMed ID: 3485955
    [Abstract] [Full Text] [Related]

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  • 8. Familial ocular anomalies in juvenile nephronophthisis.
    Godel V, Iaina A, Goldman B.
    Metab Pediatr Ophthalmol; 1980 Mar 07; 4(1):25-9. PubMed ID: 6969336
    [No Abstract] [Full Text] [Related]

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  • 10. Anthropometry of Lau Islanders, Fiji. With a note on their colour vision.
    Lourie JA.
    Hum Biol Oceania; 1972 Aug 07; 1(4):273-7. PubMed ID: 4539809
    [No Abstract] [Full Text] [Related]

  • 11. [Genetics of congenital color vision defects. II. Rare types of color blindness].
    Krawczyński MR.
    Klin Oczna; 1995 Aug 07; 97(1-2):39-43. PubMed ID: 7637312
    [Abstract] [Full Text] [Related]

  • 12. [Genetics of congenital color vision defects. I. Common types of color blindness].
    Krawczyński MR.
    Klin Oczna; 1995 Aug 07; 97(1-2):34-8. PubMed ID: 7637311
    [Abstract] [Full Text] [Related]

  • 13. Color-blindness-deficiency disease, auto-immune, or sex-linked inherited deficiency disease.
    Raymond LF.
    Eye Ear Nose Throat Mon; 1972 Apr 07; 51(4):146-7. PubMed ID: 4536869
    [No Abstract] [Full Text] [Related]

  • 14.
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  • 15. Population structure and historical genetics of isolates.
    Morton NE.
    Isr J Med Sci; 1973 Apr 07; 9(9):1299-307. PubMed ID: 4544119
    [No Abstract] [Full Text] [Related]

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  • 18. Incidence of colour-blindness among the Punjabis of India.
    Bansal IJ.
    J Genet Hum; 1967 Jun 07; 16(1):1-5. PubMed ID: 5302161
    [No Abstract] [Full Text] [Related]

  • 19. Hereditary characteristics of enzyme deficiency and dermatoglyphics in congenital color blindness.
    Wu LZ, Zeng LH, Ma QY, Xie YJ, Chen YZ, Wu DZ.
    Jpn J Ophthalmol; 1988 Jun 07; 32(2):236-45. PubMed ID: 3263528
    [Abstract] [Full Text] [Related]

  • 20. [Inheritance of color blindness].
    Waaler GH.
    Tidsskr Nor Laegeforen; 1967 Mar 01; 87(5):Suppl:468-9. PubMed ID: 5298896
    [No Abstract] [Full Text] [Related]

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