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Journal Abstract Search

78 related items for PubMed ID: 6471602

  • 21. Confirmation of the colobomatous macrophthalmia with microcornea syndrome: report of another family.
    Pallotta R, Fusilli P, Sabatino G, Verrotti A, Chiarelli F.
    Am J Med Genet; 1998 Mar 19; 76(3):252-4. PubMed ID: 9508245
    [Abstract] [Full Text] [Related]

  • 22. Macular dysplasia in congenital toxoplasmosis: report of two cases.
    Roy IS, Ghosh TH, Chowdhuri B.
    Indian J Ophthalmol; 1973 Jun 19; 21(2):63-5. PubMed ID: 4789113
    [No Abstract] [Full Text] [Related]

  • 23. Severe microcornea with anterior segment malformation in a mother and her son.
    Russell-Eggitt I, Kriss A, Restori M, Speedwell L, Thompson D, Timms C, Yu C.
    Acta Ophthalmol Scand Suppl; 1996 Jun 19; (219):27-9. PubMed ID: 8741112
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  • 24. Sorsby syndrome: a report on further generations of the original family.
    Thompson EM, Baraitser M.
    J Med Genet; 1988 May 19; 25(5):313-21. PubMed ID: 3385739
    [Abstract] [Full Text] [Related]

  • 25. [Bilateral macular pseudocoloboma associated with chronic renal insufficiency in two sisters].
    Ben Mehidi A, Massin P, Paques M, Erginay A, Gaudric A, Leys A.
    J Fr Ophtalmol; 1999 May 19; 22(6):671-5. PubMed ID: 10434203
    [Abstract] [Full Text] [Related]

  • 26. [Iris-corneal dysgenesis].
    Ignat F, Preda M, Olaru C.
    Oftalmologia; 2002 May 19; 52(1):50-4. PubMed ID: 12677801
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  • 28. [Atypical macular dysplasia. (2 clinical familial cases)].
    Rathschüler R, Kahnemann F.
    Ann Ottalmol Clin Ocul; 1970 Jul 19; 96(7):379-83. PubMed ID: 5518871
    [No Abstract] [Full Text] [Related]

  • 29. [Bilateral posterior microphthalmos associated with papillomacular fold and severe hyperopia].
    Tnacheri Ouazzani B, Guedira K, Cherkaoui LO, Ibrahimy W, Daoudi R, Mohcine Z.
    J Fr Ophtalmol; 2006 Apr 19; 29(4):e9. PubMed ID: 16885800
    [Abstract] [Full Text] [Related]

  • 30. Macular hypoplasia in familial cataracts.
    Howard CW, Smith AG, Warman R.
    J Pediatr Ophthalmol Strabismus; 1993 Apr 19; 30(3):176-7. PubMed ID: 8350228
    [No Abstract] [Full Text] [Related]

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  • 32. Novel MAF mutation in a family with congenital cataract-microcornea syndrome.
    Hansen L, Eiberg H, Rosenberg T.
    Mol Vis; 2007 Oct 18; 13():2019-22. PubMed ID: 17982426
    [Abstract] [Full Text] [Related]

  • 33. Morphological studies of extraocular muscles in cases of microcornea.
    Nath K, Gogi R, Goel BS.
    J All India Ophthalmol Soc; 1970 Apr 18; 18(1):10-4. PubMed ID: 5483062
    [No Abstract] [Full Text] [Related]

  • 34. Familial arhinia, choanal atresia, and microphthalmia.
    Thiele H, Musil A, Nagel F, Majewski F.
    Am J Med Genet; 1996 May 03; 63(1):310-3. PubMed ID: 8723126
    [Abstract] [Full Text] [Related]

  • 35. Recessive congenital total cataract with microcornea and heterozygote carrier signs caused by a novel missense CRYAA mutation (R54C).
    Khan AO, Aldahmesh MA, Meyer B.
    Am J Ophthalmol; 2007 Dec 03; 144(6):949-952. PubMed ID: 17937925
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  • 39. [Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome].
    Kamińska A, Sokołowska-Oracz A, Pawluczyk-Dyjecińska M, Szaflik JP.
    Klin Oczna; 2007 Dec 03; 109(7-9):321-6. PubMed ID: 18260289
    [Abstract] [Full Text] [Related]

  • 40. [Spectral filters as a method of therapeutic correction].
    Rozenblium IuZ, Zak PP, Ostrovskiĭ MA, Aliev AG, Smol'ianinova IL, Bora EV, Mamchits II.
    Vestn Oftalmol; 1995 Dec 03; 111(3):24-6. PubMed ID: 7483197
    [Abstract] [Full Text] [Related]

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