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Journal Abstract Search

125 related items for PubMed ID: 4993795

  • 1.
    ; . PubMed ID:
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  • 2.
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  • 3. [Clinical diagnosis of the phenotype corresponding to a ring-shaped D chromosome].
    Rethoré MO, Praud E, Le Loc'h J, Joly C, Saraux H, Aussannaire M, Lejeune J.
    Presse Med (1893); 1970 Apr 25; 78(21):955-8. PubMed ID: 4986088
    [No Abstract] [Full Text] [Related]

  • 4. [Congenital coloboma of choroid associated with microphthalmos and oligophrenia].
    Parzuchowski A, Stopczyk K.
    Klin Oczna; 1971 Apr 25; 41(2):261-4. PubMed ID: 4995811
    [No Abstract] [Full Text] [Related]

  • 5. [Oculo-dento-digital syndrome].
    Dehmel H, Brambring M.
    Arch Kinderheilkd; 1971 May 25; 183(1):76-9. PubMed ID: 4996272
    [No Abstract] [Full Text] [Related]

  • 6. Primary congenital aphakia and the rubella syndrome.
    Vermeif-Keers C.
    Teratology; 1975 Jun 25; 11(3):257-65. PubMed ID: 807986
    [Abstract] [Full Text] [Related]

  • 7. [Congenital toxoplasmosis, microphthalmia and coloboma of the optic nerve].
    Constantin F.
    Rev Med Chir Soc Med Nat Iasi; 1974 Jun 25; 78(3):719-22. PubMed ID: 4476916
    [No Abstract] [Full Text] [Related]

  • 8.
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  • 9. [Congenital hyaloid-retinal dysplasias and their differential diagnosis].
    Ricci A.
    J Genet Hum; 1969 Jun 25; ():Suppl 7:1-191. PubMed ID: 4996588
    [No Abstract] [Full Text] [Related]

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  • 11. The ocular findings in the trisomy syndromes.
    Keith CG.
    Proc R Soc Med; 1968 Mar 25; 61(3):251-3. PubMed ID: 4967114
    [No Abstract] [Full Text] [Related]

  • 12. Microphthalmia in triploid chicken embryos from the morphogenetical point of view.
    Slipka J.
    Folia Morphol (Praha); 1973 Mar 25; 21(2):118-20. PubMed ID: 4750367
    [No Abstract] [Full Text] [Related]

  • 13. A family with microphthalmia, anophthalmia and concomitant oligophrenia.
    Bianchine JW.
    Birth Defects Orig Artic Ser; 1971 Mar 25; 7(3):205-6. PubMed ID: 5173148
    [No Abstract] [Full Text] [Related]

  • 14. [Ocular abnormalities of phenotype DR (ring D chromosome)].
    Saraux H, Réthoré MO, Aussannaire M, Dhermy P, Joly C, Le Loch J, Praud E, Lejeune J.
    Ann Ocul (Paris); 1970 Aug 25; 203(8):737-48. PubMed ID: 4992291
    [No Abstract] [Full Text] [Related]

  • 15. Ocular anomalies associated with interstitial deletion of chromosome 2q31: case report and review.
    Gambrelle J, Till M, Lukusa B, Beby F, Mory N, Sann L, Kodjikian L, Grange JD, Putet G.
    Ophthalmic Genet; 2007 Jun 25; 28(2):105-9. PubMed ID: 17558854
    [Abstract] [Full Text] [Related]

  • 16. Hydrocephaly, congenital retinal nonattachment, and congenital falciform fold.
    Warburg M.
    Am J Ophthalmol; 1978 Jan 25; 85(1):88-94. PubMed ID: 413438
    [Abstract] [Full Text] [Related]

  • 17. Syndromes and systemic diseases with eye findings.
    Sargent RA.
    Pediatrician; 1990 Jan 25; 17(3):183-93. PubMed ID: 2194183
    [Abstract] [Full Text] [Related]

  • 18. [Brain malformation and mental retardation].
    Murofushi K.
    Shinkei Kenkyu No Shimpo; 1972 Apr 25; 16(2):218-25. PubMed ID: 4260443
    [No Abstract] [Full Text] [Related]

  • 19. Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
    Ng D, Hadley DW, Tifft CJ, Biesecker LG.
    Am J Med Genet; 2002 Jul 15; 110(4):308-14. PubMed ID: 12116202
    [Abstract] [Full Text] [Related]

  • 20. Lenz microphthalmia syndrome: three additional cases with rare associated anomalies.
    Temtamy SA, Ismail SI, Meguid NA.
    Genet Couns; 2000 Jul 15; 11(2):147-52. PubMed ID: 10893665
    [Abstract] [Full Text] [Related]

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