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Journal Abstract Search

161 related items for PubMed ID: 4543802

  • 1. [Genetic counseling in eye diseases (author's transl)].
    Burow B, Theile U.
    Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1973 Nov 06; 188(4):307-21. PubMed ID: 4543802
    [No Abstract] [Full Text] [Related]

  • 2. [Useful data in genetic counseling].
    François J.
    Ann Ocul (Paris); 1972 Nov 06; 205(11):1173-80. PubMed ID: 4196608
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  • 3. [Genetic prognosis in ophthalmology].
    François J.
    Annee Ther Clin Ophtalmol; 1972 Nov 06; 23():319-30. PubMed ID: 4680285
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  • 12. Karyotype studies among children with severe visual handicap.
    Fraser GR, Friedmann AI, Delhanty JD, Edwards JH, Glen-Bott AM, Insley J, Lele KP, Mittwoch U, Mutton D.
    Br J Ophthalmol; 1970 Feb 06; 54(2):79-89. PubMed ID: 5441784
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  • 13. Molecular biology in ocular disorders.
    Keith CG.
    Med J Aust; 1993 May 03; 158(9):615-8. PubMed ID: 8479380
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  • 14. [Cytogenetic studies in children with visual disorders].
    Muşeţeanu P, Garoiu M, Duca-Marinescu D, Carangiu M, Friciu E, Ionescu B, Maximilian C.
    Stud Cercet Endocrinol; 1972 May 03; 23(5):333-5. PubMed ID: 4219458
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  • 16. [Investigative studies on some blinding hereditary eye diseases (author's transl)].
    Cao DJ.
    Zhonghua Yan Ke Za Zhi; 1981 Jul 03; 17(4):233-6. PubMed ID: 6802615
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  • 20. New phenotype associated with an Arg116Cys mutation in the CRYAA gene: nuclear cataract, iris coloboma, and microphthalmia.
    Beby F, Commeaux C, Bozon M, Denis P, Edery P, Morlé L.
    Arch Ophthalmol; 2007 Feb 03; 125(2):213-6. PubMed ID: 17296897
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