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PUBMED FOR HANDHELDS

Journal Abstract Search


243 related items for PubMed ID: 7246606

  • 21. Diagnostic precision in microphthalmos and coloboma of heterogeneous origin.
    Warburg M.
    Birth Defects Orig Artic Ser; 1982; 18(6):31-50. PubMed ID: 7171763
    [Abstract] [Full Text] [Related]

  • 22. Ptosis, coloboma, hypertelorism and mental retardation.
    Warburg M.
    Genet Couns; 1993; 4(1):69-70. PubMed ID: 8471225
    [No Abstract] [Full Text] [Related]

  • 23. BBBG syndrome or Opitz syndrome: new family.
    Verloes A, Le Merrer M, Briard ML.
    Am J Med Genet; 1989 Nov; 34(3):313-6. PubMed ID: 2688419
    [Abstract] [Full Text] [Related]

  • 24. Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome.
    Baraitser M, Winter RM.
    J Med Genet; 1988 Jan; 25(1):41-3. PubMed ID: 3351890
    [Abstract] [Full Text] [Related]

  • 25. Ocular hypotelorism, submucosal cleft palate, and hypospadias: a new autosomal dominant syndrome.
    Schilbach U, Rott HD.
    Am J Med Genet; 1988 Dec; 31(4):863-70. PubMed ID: 3149147
    [Abstract] [Full Text] [Related]

  • 26. Silver staining of the supernumerary chromosome in the cat-eye syndrome.
    Petit P, Godart S, Fryns JP.
    Ann Genet; 1980 Dec; 23(2):114-6. PubMed ID: 6156636
    [Abstract] [Full Text] [Related]

  • 27. The "cat eye" syndrome--report of a case with hypothyroidism.
    Ioan D, Dumitriu L, Fabriţius K, Simescu M, Maximilian C.
    Endocrinologie; 1986 Dec; 24(2):129-31. PubMed ID: 3738402
    [Abstract] [Full Text] [Related]

  • 28. Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome possibly localised on chromosome 2.
    Pallotta R.
    J Med Genet; 1991 May; 28(5):342-4. PubMed ID: 1865474
    [Abstract] [Full Text] [Related]

  • 29. Autosomal dominant piebaldism and mental retardation syndrome associated with a t(1;2) (p22.1;q36).
    Rivera H, Alvarez-Arratia MC, Moller M, Tinoco-Contreras M, Flores-Perez A, Cantu JM.
    J Genet Hum; 1986 Aug; 34(3-4):321-5. PubMed ID: 3760835
    [Abstract] [Full Text] [Related]

  • 30. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
    Vieira H, Gregory-Evans K, Lim N, Brookes JL, Brueton LA, Gregory-Evans CY.
    Invest Ophthalmol Vis Sci; 2002 Aug; 43(8):2540-5. PubMed ID: 12147582
    [Abstract] [Full Text] [Related]

  • 31. Brief clinical report: dup(4p15 leads to 4pter) in a 19-year-old woman resulting from a maternal 4;14 translocation.
    Clark CE, Telfer MA, Cowell HR, Kalamchi A, Steg NL.
    Am J Med Genet; 1982 Jan; 11(1):37-42. PubMed ID: 7065001
    [Abstract] [Full Text] [Related]

  • 32. The Marinesco-Sjögren syndrome: polygraphic study of nocturnal sleep.
    Bramanti P, Ricci RM, Benedetto M, Candela L, Bagalà S, Di Perri R.
    Acta Neurol (Napoli); 1985 Feb; 7(1):8-13. PubMed ID: 3993461
    [No Abstract] [Full Text] [Related]

  • 33. Dominant inheritance of holoprosencephaly.
    Cantú JM, Fragoso R, Garcia-Cruz D, Sánchez-Corona J.
    Birth Defects Orig Artic Ser; 1978 Feb; 14(6B):215-20. PubMed ID: 728563
    [No Abstract] [Full Text] [Related]

  • 34. G syndrome (hypertelorism with esophageal abnormality and hypospadias, or hypospadias-dysphagia, or "Opitz-Frias" or "Opitz-G" syndrome)--perspective in 1987 and bibliography.
    Opitz JM.
    Am J Med Genet; 1987 Oct; 28(2):275-85. PubMed ID: 3322001
    [No Abstract] [Full Text] [Related]

  • 35. De novo ring chromosome 3 in a girl with hypoplastic thumb and coloboma of iris.
    Barajas-Barajas LO, Velarde-Félix S, Elizarrarás-Rivas J, Hernández-Zaragoza G, Vázquez-Herrera JA.
    Genet Couns; 2001 Oct; 12(2):151-6. PubMed ID: 11491310
    [Abstract] [Full Text] [Related]

  • 36. SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.
    Gregory-Evans CY, Moosajee M, Hodges MD, Mackay DS, Game L, Vargesson N, Bloch-Zupan A, Rüschendorf F, Santos-Pinto L, Wackens G, Gregory-Evans K.
    Hum Mol Genet; 2007 Oct 15; 16(20):2482-93. PubMed ID: 17656375
    [Abstract] [Full Text] [Related]

  • 37. [Familial occurrence of congenital aniridia].
    Zalewska R, Midro AT, Bakunowicz-Lazarczyk A, Proniewska-Skretek E.
    Klin Oczna; 1992 Oct 15; 94(5-6):159-60. PubMed ID: 1453680
    [Abstract] [Full Text] [Related]

  • 38. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.
    Wieczorek D, Krause M, Majewski F, Albrecht B, Horn D, Riess O, Gillessen-Kaesbach G.
    Eur J Hum Genet; 2000 Jul 15; 8(7):519-26. PubMed ID: 10909852
    [Abstract] [Full Text] [Related]

  • 39. Autosomal dominant typical coloboma associated with unilateral pseudoptosis, myopia and cataract.
    Porges Y.
    Cent Afr J Med; 1995 Aug 15; 41(8):255-7. PubMed ID: 7585914
    [Abstract] [Full Text] [Related]

  • 40. Corneal changes in familial iris coloboma.
    Soong HK, Raizman MB.
    Ophthalmology; 1986 Mar 15; 93(3):335-9. PubMed ID: 3703500
    [Abstract] [Full Text] [Related]


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