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Journal Abstract Search

114 related items for PubMed ID: 8669446

  • 1. Additional case of craniofacial and digital anomalies as reported by Harrod et al.
    Jurenka SB, Van Allen MI.
    Am J Med Genet; 1996 Jan 11; 61(2):168-70. PubMed ID: 8669446
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  • 2. Megadolichosigmoid in a young male with Aarskog syndrome.
    Casteels M, Samain H, Penninckx F, Coremans G, Beirinckx J, Fryns JP.
    Genet Couns; 1994 Jan 11; 5(1):81-3. PubMed ID: 8031541
    [No Abstract] [Full Text] [Related]

  • 3. Kabuki make-up syndrome and hearing impairment.
    Say B, McCutcheon L, Todd C, Hough JV.
    Clin Dysmorphol; 1993 Jan 11; 2(1):68-70. PubMed ID: 8298741
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  • 4. Smith-Fineman-Myers syndrome: report of a third case.
    Stephenson LD, Johnson JP.
    Am J Med Genet; 1985 Oct 11; 22(2):301-4. PubMed ID: 4050861
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  • 6. Fragile X family with unusual digital and facial abnormalities, cleft lip and palate, and epilepsy.
    Loesch DZ, Hay DA, Sheffield LJ.
    Am J Med Genet; 1992 Nov 15; 44(5):543-50. PubMed ID: 1481805
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  • 7. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation.
    Kelly TE, Kirson L, Wyatt J.
    Am J Med Genet; 1993 Feb 01; 45(3):353-5. PubMed ID: 8434622
    [Abstract] [Full Text] [Related]

  • 8. Oto-palato-digital syndrome with features of type I and II in brothers.
    Horn D, Nitz I, Bollmann R.
    Genet Couns; 1995 Feb 01; 6(3):233-40. PubMed ID: 8588852
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  • 10. Fryns syndrome: another example of non-lethal outcome with severe mental handicap.
    Hanssen AM, Schrander-Stumpel CT, Thiry PA, Fryns JP.
    Genet Couns; 1992 Feb 01; 3(4):187-93. PubMed ID: 1472353
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  • 14. [Coffin-Siris syndrome in a 5-year-old girl].
    Meinecke P, Engelbrecht R, Schaefer E.
    Monatsschr Kinderheilkd; 1986 Sep 01; 134(9):692-5. PubMed ID: 3785238
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  • 15. Floating-Harbor syndrome: case report.
    Genc G, Sarac A, Erkek Atay N, Kulali F.
    Minerva Pediatr; 2008 Apr 01; 60(2):249-51. PubMed ID: 18449141
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  • 16. Characteristic facial dysmorphism, arachnodactyly and mental retardation: another case.
    Van Buggenhout GJ, Akkermans-Scholten AC, Hamel BC.
    Genet Couns; 1995 Apr 01; 6(1):61-3. PubMed ID: 7794564
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  • 18. Kabuki syndrome and diaphragmatic defect.
    Sethi SK, Faridi MM.
    Indian Pediatr; 2006 Jun 01; 43(6):552-3. PubMed ID: 16820668
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  • 20. The craniodigital syndrome of Scott: report of a second family.
    Lorenz P, Hinkel GK, Hoffmann C, Rupprecht E.
    Am J Med Genet; 1990 Oct 01; 37(2):224-6. PubMed ID: 2174209
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