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Journal Abstract Search

179 related items for PubMed ID: 8256802

  • 1. Váradi syndrome (OFD VI) or Opitz trigonocephaly syndrome: overlapping manifestations in two cousins.
    Cleper R, Kauschansky A, Varsano I, Frydman M.
    Am J Med Genet; 1993 Sep 15; 47(4):451-5. PubMed ID: 8256802
    [Abstract] [Full Text] [Related]

  • 2. Varadi syndrome or Opitz trigonocephaly: overlapping manifestation in two cousins.
    Bankier A, Rose CM.
    Am J Med Genet; 1994 Oct 15; 53(1):85-8. PubMed ID: 7802045
    [No Abstract] [Full Text] [Related]

  • 3. Opitz trigonocephaly syndrome.
    Haaf T, Hofmann R, Schmid M.
    Am J Med Genet; 1991 Sep 15; 40(4):444-6. PubMed ID: 1746609
    [Abstract] [Full Text] [Related]

  • 4. [Opitz-trigonocephaly syndrome--a characteristic dysmorphia-retardation syndrome of unclear origin].
    Choudhury AR, Renneberg A, Rackowitz A, Stephani U.
    Klin Padiatr; 1992 Sep 15; 204(3):171-3. PubMed ID: 1614184
    [Abstract] [Full Text] [Related]

  • 5. A new X-linked multiple congenital anomalies/mental retardation syndrome.
    Golabi M, Ito M, Hall BD.
    Am J Med Genet; 1984 Jan 15; 17(1):367-74. PubMed ID: 6711604
    [Abstract] [Full Text] [Related]

  • 6. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
    Hamel BC, Mariman EC, van Beersum SE, Schoonbrood-Lenssen AM, Ropers HH.
    Am J Med Genet; 1994 Jul 15; 51(4):591-7. PubMed ID: 7943045
    [Abstract] [Full Text] [Related]

  • 7. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.
    Terespolsky D, Farrell SA, Siegel-Bartelt J, Weksberg R.
    Am J Med Genet; 1995 Nov 20; 59(3):329-33. PubMed ID: 8599356
    [Abstract] [Full Text] [Related]

  • 8. Further delineation of the C (trigonocephaly) syndrome.
    Antley RM, Hwang DS, Theopold W, Gorlin RJ, Steeper T, Pitt D, Danks DM, McPherson E, Bartels H, Wiedemann HR, Opitz JM.
    Am J Med Genet; 1981 Nov 20; 9(2):147-63. PubMed ID: 7258228
    [Abstract] [Full Text] [Related]

  • 9. Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality.
    Curry CJ, Carey JC, Holland JS, Chopra D, Fineman R, Golabi M, Sherman S, Pagon RA, Allanson J, Shulman S.
    Am J Med Genet; 1987 Jan 20; 26(1):45-57. PubMed ID: 3812577
    [Abstract] [Full Text] [Related]

  • 10. Kabuki make-up (Niikawa-Kuroki) syndrome in five Spanish children.
    Galán-Gómez E, Cardesa-García JJ, Campo-Sampedro FM, Salamanca-Maesso C, Martínez-Frías ML, Frías JL.
    Am J Med Genet; 1995 Nov 20; 59(3):276-82. PubMed ID: 8599349
    [Abstract] [Full Text] [Related]

  • 11. Another Arab patient with overlap of Váradi-Papp/Opitz trigonocephaly syndromes?
    Sabry MA, al Saleh Q, Farah S, Obenbergerova D, Simeonov S, al Awadi SA, Farag TI.
    Am J Med Genet; 1997 Jan 10; 68(1):54-7. PubMed ID: 8986276
    [Abstract] [Full Text] [Related]

  • 12. Opitz-C syndrome: on the nosology of mental retardation and trigonocephaly.
    Schaap C, Schrander-Stumpel CT, Fryns JP.
    Genet Couns; 1992 Jan 10; 3(4):209-15. PubMed ID: 1472356
    [Abstract] [Full Text] [Related]

  • 13. Brief clinical report: two children with de novo del(9p).
    Young RS, Bader P, Palmer CG, Kaler SG, Hodes ME.
    Am J Med Genet; 1983 Apr 10; 14(4):751-7. PubMed ID: 6846405
    [Abstract] [Full Text] [Related]

  • 14. BBBG syndrome or Opitz syndrome: new family.
    Verloes A, Le Merrer M, Briard ML.
    Am J Med Genet; 1989 Nov 10; 34(3):313-6. PubMed ID: 2688419
    [Abstract] [Full Text] [Related]

  • 15. Cardio-facio-cutaneous (CFC) syndrome: report of a new patient.
    Chrzanowska K, Fryns JP, Van den Berghe H.
    Am J Med Genet; 1989 Aug 10; 33(4):471-3. PubMed ID: 2596505
    [Abstract] [Full Text] [Related]

  • 16. [Molecular diagnosis of CHARGE syndrom].
    Pedersen AM, Skovby F.
    Ugeskr Laeger; 2007 Jan 29; 169(5):402-6. PubMed ID: 17280632
    [Abstract] [Full Text] [Related]

  • 17. An anatomical study of a duplication 6p based on two sibs.
    Smith BS, Pettersen JC.
    Am J Med Genet; 1985 Apr 29; 20(4):649-63. PubMed ID: 3993686
    [Abstract] [Full Text] [Related]

  • 18. Acrocallosal syndrome in a girl born to consanguineous parents.
    Salgado LJ, Ali CA, Castilla EE.
    Am J Med Genet; 1989 Mar 29; 32(3):298-300. PubMed ID: 2729348
    [Abstract] [Full Text] [Related]

  • 19. Biochemical abnormality associated with Smith-Lemli-Opitz syndrome in an infant with features of Rutledge multiple congenital anomaly syndrome confirms that the latter is a variant of the former.
    Rakheja D, Wilson GN, Rogers BB.
    Pediatr Dev Pathol; 2003 Mar 29; 6(3):270-7. PubMed ID: 12717589
    [Abstract] [Full Text] [Related]

  • 20. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML, Pai GS, Wilkes B, Lebel RR.
    Am J Med Genet; 2001 Aug 15; 102(3):237-42. PubMed ID: 11484200
    [Abstract] [Full Text] [Related]

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