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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

122 related items for PubMed ID: 7307870

  • 21. Inheritance of congenital esotropia.
    Maumenee IH, Alston A, Mets MB, Flynn JT, Mitchell TN, Beaty TH.
    Trans Am Ophthalmol Soc; 1986; 84():85-93. PubMed ID: 3590483
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  • 24. Progressive external ophthalmoplegia associated with retinal pigment epitheliopathy.
    Daniele S, Cianchetti C, Cao A.
    Am J Ophthalmol; 1975 Oct; 80(4):585-90. PubMed ID: 1180302
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  • 25. Inheritance in the etiology of convergent squint.
    Dufier JL, Briard ML, Bonaiti C, Frezal J, Saraux H.
    Ophthalmologica; 1979 Oct; 179(4):225-34. PubMed ID: 548860
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  • 27. Dominant optic nerve atrophy with progressive hearing loss and chronic progressive external ophthalmoplegia (CPEO).
    Meire F, De Laey JJ, de Bie S, van Staey M, Matton MT.
    Ophthalmic Paediatr Genet; 1985 Feb; 5(1-2):91-7. PubMed ID: 4058877
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  • 28. New autosomal dominant radial ray hypoplasia syndrome.
    Goldblatt J, Viljoen D.
    Am J Med Genet; 1987 Nov; 28(3):647-54. PubMed ID: 3425633
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  • 29. Vitreoretinal degeneration as a sign of generalized connective tissue diseases.
    Maumenee IH.
    Am J Ophthalmol; 1979 Sep; 88(3 Pt 1):432-49. PubMed ID: 114056
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  • 31. [Abundant familial occurrence of strabismus amblyopia (author's transl)].
    Aichmair H.
    Klin Monbl Augenheilkd; 1980 Feb; 176(2):276-8. PubMed ID: 7420979
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  • 32. [A case of pseudoparetic strabismus].
    Baranowska-George T, Tokarz-Sawińska E, Kugler R.
    Klin Oczna; 1987 Feb; 89(2):71-4. PubMed ID: 3669520
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  • 40. High myopia, retinal dystrophy, and mental retardation in siblings.
    Hayasaka S, Fujitani A, Noda S, Setogawa T.
    Ann Ophthalmol; 1994 Feb; 26(2):39-41. PubMed ID: 8010702
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