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Journal Abstract Search

467 related items for PubMed ID: 7617402

  • 1. Peters'-Plus syndrome: report on an unusual case.
    Camera G, Pozzolo S, Carta M, Righi E.
    Pathologica; 1994 Dec; 86(6):673-5. PubMed ID: 7617402
    [Abstract] [Full Text] [Related]

  • 2. Kivlin syndrome and Peters'-Plus syndrome: are they the same disorder?
    Thompson EM, Winter RM, Baraitser M.
    Clin Dysmorphol; 1993 Oct; 2(4):301-16. PubMed ID: 7508317
    [Abstract] [Full Text] [Related]

  • 3. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G, Centa A, Pozzolo S, Camera A.
    Clin Dysmorphol; 1993 Oct; 2(4):317-21. PubMed ID: 8305962
    [Abstract] [Full Text] [Related]

  • 4. The Peters'-Plus syndrome: description of 16 patients and review of the literature.
    Hennekam RC, Van Schooneveld MJ, Ardinger HH, Van Den Boogaard MJ, Friedburg D, Rudnik-Schoneborn S, Seguin JH, Weatherstone KB, Wittebol-Post D, Meinecke P.
    Clin Dysmorphol; 1993 Oct; 2(4):283-300. PubMed ID: 7508316
    [Abstract] [Full Text] [Related]

  • 5. Dysgenesis mesodermalis of the cornea (Peters' anomaly) associated with cleft lip and palate.
    Ide CH, Matta C, Holt JE, Felker GV.
    Ann Ophthalmol; 1975 Jun; 7(6):841-2. PubMed ID: 1147511
    [No Abstract] [Full Text] [Related]

  • 6. [Nasal dermoid sinus cyst: accidental coincidence or syndrome association?].
    Pausch NC, Frerich B, Hemprich A, Brylla E, Sterker I, Merkenschlager A.
    Klin Padiatr; 2008 Jun; 220(5):321-4. PubMed ID: 18401812
    [Abstract] [Full Text] [Related]

  • 7. The Peters' plus syndrome: a review.
    Maillette de Buy Wenniger-Prick LJ, Hennekam RC.
    Ann Genet; 2002 Jun; 45(2):97-103. PubMed ID: 12119218
    [Abstract] [Full Text] [Related]

  • 8. Surgical management of glaucoma in infants and children with Peters' anomaly: long-term structural and functional outcome.
    Yang LL, Lambert SR, Lynn MJ, Stulting RD.
    Ophthalmology; 2004 Jan; 111(1):112-7. PubMed ID: 14711722
    [Abstract] [Full Text] [Related]

  • 9. Peters anomaly in association with multiple midline anomalies and a familial chromosome 4 inversion.
    Neilan E, Pikman Y, Kimonis VE.
    Ophthalmic Genet; 2006 Jun; 27(2):63-5. PubMed ID: 16754208
    [Abstract] [Full Text] [Related]

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  • 11. Congenital hypothyroidism in Peters plus syndrome.
    Kosaki R, Kamiishi A, Sugiyama R, Kawai M, Hasegawa T, Kosaki K.
    Ophthalmic Genet; 2006 Jun; 27(2):67-9. PubMed ID: 16754209
    [Abstract] [Full Text] [Related]

  • 12. Anterior chamber cleavage syndrome. A typical case of Peters' anomaly with primary aphakia.
    Holmark J, Jensen OA.
    Acta Ophthalmol (Copenh); 1972 Jun; 50(6):877-86. PubMed ID: 4631516
    [No Abstract] [Full Text] [Related]

  • 13. Foxe3 haploinsufficiency in mice: a model for Peters' anomaly.
    Ormestad M, Blixt A, Churchill A, Martinsson T, Enerbäck S, Carlsson P.
    Invest Ophthalmol Vis Sci; 2002 May; 43(5):1350-7. PubMed ID: 11980846
    [Abstract] [Full Text] [Related]

  • 14. [Familiary arhinia combined with peters' anomaly and maxilliar deformities, a new malformation syndrome (author's transl)].
    Ruprecht KW, Majewski F.
    Klin Monbl Augenheilkd; 1978 May; 172(5):708-15. PubMed ID: 672092
    [Abstract] [Full Text] [Related]

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  • 16. Optimising keratoplasty for Peters' anomaly in infants using spectral-domain optical coherence tomography.
    Hong J, Yang Y, Cursiefen C, Mashaghi A, Wu D, Liu Z, Sun X, Dana R, Xu J.
    Br J Ophthalmol; 2017 Jun; 101(6):820-827. PubMed ID: 27660330
    [Abstract] [Full Text] [Related]

  • 17. Neuhauser syndrome and Peters' anomaly.
    Yarar C, Yakut A, Yildirim N, Yildiz B, Basmak H.
    Clin Dysmorphol; 2006 Oct; 15(4):249-251. PubMed ID: 16957485
    [Abstract] [Full Text] [Related]

  • 18. Peters' anomaly as a consequence of genetic and nongenetic syndromes.
    Kivlin JD, Fineman RM, Crandall AS, Olson RJ.
    Arch Ophthalmol; 1986 Jan; 104(1):61-4. PubMed ID: 3079999
    [Abstract] [Full Text] [Related]

  • 19. Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients.
    Niikawa N, Kuroki Y, Kajii T, Matsuura N, Ishikiriyama S, Tonoki H, Ishikawa N, Yamada Y, Fujita M, Umemoto H.
    Am J Med Genet; 1988 Nov; 31(3):565-89. PubMed ID: 3067577
    [Abstract] [Full Text] [Related]

  • 20. Dental evaluation of Kabuki syndrome patients.
    Teixeira CS, Silva CR, Honjo RS, Bertola DR, Albano LM, Kim CA.
    Cleft Palate Craniofac J; 2009 Nov; 46(6):668-73. PubMed ID: 19860501
    [Abstract] [Full Text] [Related]

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