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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

190 related items for PubMed ID: 4996588

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  • 29. [Partial trisomy C by t(Cp-; B+) translocation].
    De Grouchy J, Roy C, Lachance R, Frezal J, Lamy M.
    Arch Fr Pediatr; 1967 Oct; 24(8):849-58. PubMed ID: 5584188
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  • 30. [Partial trisomy C through a familial translocation t(Cq+;Cq-)].
    Lejeune J, Rethoré MO, Berger R, Abonyi D, Dutrillaux B, See G.
    Ann Genet; 1968 Sep; 11(3):171-5. PubMed ID: 5304617
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  • 31. Study of the Norrie disease gene in 2 patients with bilateral persistent hyperplastic primary vitreous.
    Pendergast SD, Trese MT, Liu X, Shastry BS.
    Arch Ophthalmol; 1998 Mar; 116(3):381-2. PubMed ID: 9514496
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  • 32. [Congenital toxoplasmosis with atypical detachment and necrosis of the retina, persistence of the primary vitreous body, additional abnormalities and extensive intraocular ectopic hematopoiesis].
    Gloor B, Haller R.
    Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1968 Mar; 175(3):193-207. PubMed ID: 5302229
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  • 33. The extra digit. A pointer to the eye?
    Calver D, Keast-Butler J, Taylor D.
    Trans Ophthalmol Soc U K (1962); 1981 Mar; 101(1):35-8. PubMed ID: 6821009
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  • 34. [Ocular manifestations of trisomy D1. Clinical and histopathological study].
    François J, Hanssens M.
    Ann Ocul (Paris); 1970 Oct; 203(10):873-914. PubMed ID: 4993043
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  • 35. [Persistence of the primordial vitreous body and buphthalmos].
    Cernea P, Simionescu C, Bosun I.
    Oftalmologia; 1995 Oct; 39(4):338-42. PubMed ID: 7577904
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  • 36. Persistent hyperplastic primary vitreous of the eye: imaging findings with pathologic correlation.
    Kaste SC, Jenkins JJ, Meyer D, Fontanesi J, Pratt CB.
    AJR Am J Roentgenol; 1994 Feb; 162(2):437-40. PubMed ID: 8310942
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  • 37. [Trisomy 18].
    Berger R.
    Nouv Presse Med; 1972 Mar 11; 1(11):745-8. PubMed ID: 5022253
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  • 38. Electromyographic characteristics of congenital and early onset motor unit diseases.
    Fowler WM, Taylor RG, Munsat TL.
    Arch Phys Med Rehabil; 1971 Aug 11; 52(8):343-61. PubMed ID: 5284447
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  • 39. [Retinal abnormalities in three genetic disorders involving the X chromosome].
    Falfoul Y, El Leuch IE, El Matri K, Chaker N, El Matri L.
    J Fr Ophtalmol; 2020 Dec 11; 43(10):1107-1108. PubMed ID: 32829937
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  • 40. Sectoral iris heterochromia and retinal pigment variation in 13q-syndrome.
    Kutzbach B, Mendelsohn N, Rath P, Summers CG.
    J AAPOS; 2007 Oct 11; 11(5):513-5. PubMed ID: 17933676
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