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Journal Abstract Search

200 related items for PubMed ID: 11528734

  • 1. [Naso-digital-acoustic syndrome, Keipert type].
    Yamaguchi K, Kondoh T.
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):270. PubMed ID: 11528734
    [No Abstract] [Full Text] [Related]

  • 2. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
    Filippi G.
    Am J Med Genet; 1985 Dec; 22(4):821-4. PubMed ID: 4073130
    [Abstract] [Full Text] [Related]

  • 3. Six patients with oral-facial-digital syndrome IV: the case for heterogeneity.
    Toriello HV, Carey JC, Suslak E, Desposito FR, Leonard B, Lipson M, Friedman BD, Hoyme HE.
    Am J Med Genet; 1997 Mar 31; 69(3):250-60. PubMed ID: 9096753
    [Abstract] [Full Text] [Related]

  • 4. Possible new type of oral-facial-digital syndrome with retinal abnormalities: OFDS type (VIII).
    Gurrieri F, Sammito V, Ricci B, Iossa M, Bellussi A, Neri G.
    Am J Med Genet; 1992 Apr 01; 42(6):789-92. PubMed ID: 1554016
    [Abstract] [Full Text] [Related]

  • 5. [Coffin-Siris syndrome. Critical study of the literature apropos of a case].
    Foasso MF, Hermier M, Descos B, Collet JP, Perron F.
    Pediatrie; 1983 Mar 01; 38(2):111-7. PubMed ID: 6622139
    [Abstract] [Full Text] [Related]

  • 6. Extending the Pallister-Hall syndrome to include other central nervous system malformations.
    Finnigan DP, Clarren SK, Haas JE.
    Am J Med Genet; 1991 Sep 15; 40(4):395-400. PubMed ID: 1746599
    [Abstract] [Full Text] [Related]

  • 7. Additional case of Keipert syndrome and review of the literature.
    Cappon SM, Khalifa MM.
    Med Sci Monit; 2000 Sep 15; 6(4):776-8. PubMed ID: 11208408
    [Abstract] [Full Text] [Related]

  • 8. Rubinstein-Taybi syndrome.
    Gellis SS, Feingold M.
    Am J Dis Child; 1971 Apr 15; 121(4):327-8. PubMed ID: 5550739
    [No Abstract] [Full Text] [Related]

  • 9. [Börjeson-Forssman-Lehmann syndrome].
    Kubota T.
    Nihon Rinsho; 2006 Sep 28; Suppl 3():410-2. PubMed ID: 17022575
    [No Abstract] [Full Text] [Related]

  • 10. [Oto-palato-digital syndrome, type II].
    Narahara K.
    Ryoikibetsu Shokogun Shirizu; 2001 Sep 28; (34 Pt 2):446-8. PubMed ID: 11528829
    [No Abstract] [Full Text] [Related]

  • 11. Kabuki syndrome: description of a 2-year old Roumanian boy and review of the literature.
    Ioan DM, Fryns JP.
    Genet Couns; 2007 Sep 28; 18(1):113-7. PubMed ID: 17515307
    [Abstract] [Full Text] [Related]

  • 12. [Oculo-dento-digital syndrome. (Oculo-dento-digital dysplasia)].
    Vittori F, Carbonnel Y.
    Pediatrie; 1976 Sep 28; 31(6):593-601. PubMed ID: 826871
    [No Abstract] [Full Text] [Related]

  • 13. [Trichorhinophalangeal syndrome : analysis of craniofacial architecture in six cases (author's transl)].
    Scheffer P, Verdier M, Finidori G.
    Rev Stomatol Chir Maxillofac; 1981 Sep 28; 82(4):230-3. PubMed ID: 6944759
    [Abstract] [Full Text] [Related]

  • 14. Hereditary sensorineural hearing loss associated with onychodystrophy and digital malformations.
    Moghadam H, Statten P.
    Can Med Assoc J; 1972 Aug 19; 107(4):310-2. PubMed ID: 5056117
    [No Abstract] [Full Text] [Related]

  • 15. Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28.
    Amor DJ, Dahl HH, Bahlo M, Bankier A.
    Am J Med Genet A; 2007 Oct 01; 143A(19):2236-41. PubMed ID: 17726694
    [Abstract] [Full Text] [Related]

  • 16. [Unusual case of ocular and digital changes classifiable as oculodentodigital dysplasia].
    Gemme G, Bonioli E, Ruffa G, Grosso P.
    Minerva Pediatr; 1976 Nov 10; 28(35):2155-60. PubMed ID: 1012235
    [No Abstract] [Full Text] [Related]

  • 17. A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity.
    Cataltepe S, Tuncbilek E.
    Eur J Pediatr; 1992 Apr 10; 151(4):288-90. PubMed ID: 1499582
    [Abstract] [Full Text] [Related]

  • 18. Characteristic facies in type B brachydactyly?
    Houlston RS, Temple IK.
    Clin Dysmorphol; 1994 Jul 10; 3(3):224-7. PubMed ID: 7981857
    [Abstract] [Full Text] [Related]

  • 19. [Oto-palato-digital syndrome, type I].
    Narahara K.
    Ryoikibetsu Shokogun Shirizu; 2001 Jul 10; (34 Pt 2):444-5. PubMed ID: 11528828
    [No Abstract] [Full Text] [Related]

  • 20. Short-rib-polydactyly syndrome (Saldino-Noonan type).
    Pirnar T, Balci S, Cağlar M.
    Turk J Pediatr; 1982 Jul 10; 24(3):175-82. PubMed ID: 7147365
    [No Abstract] [Full Text] [Related]

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