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Journal Abstract Search

103 related items for PubMed ID: 8986276

  • 1. 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]

  • 2. 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]

  • 3. Opitz C trigonocephaly syndrome and midline brain anomalies.
    Zampino G, Di Rocco C, Butera G, Balducci F, Colosimo C, Torrioli MG, Mastroiacovo P.
    Am J Med Genet; 1997 Dec 31; 73(4):484-8. PubMed ID: 9415479
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  • 4. Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family.
    Marafie MJ, Temtamy SA, Rajaram U, al-Awadi SA, el-Badramany MH, Farag TI.
    Am J Med Genet; 1996 Dec 18; 66(3):261-4. PubMed ID: 8985483
    [Abstract] [Full Text] [Related]

  • 5. Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?
    Bohring A, Silengo M, Lerone M, Superneau DW, Spaich C, Braddock SR, Poss A, Opitz JM.
    Am J Med Genet; 1999 Aug 27; 85(5):438-46. PubMed ID: 10405439
    [Abstract] [Full Text] [Related]

  • 6. OFD II, OFD VI, and Joubert syndrome manifestations in 2 sibs.
    Haug K, Khan S, Fuchs S, König R.
    Am J Med Genet; 2000 Mar 13; 91(2):135-7. PubMed ID: 10748413
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum.
    Guzzetta V, Lecora M, Rossi G, Berni Canani M, Andria G.
    Clin Dysmorphol; 1996 Apr 15; 5(2):179-82. PubMed ID: 8723570
    [Abstract] [Full Text] [Related]

  • 9. Plantar lipomatosis, unusual facial phenotype and developmental delay: a new MCA/MR syndrome.
    Pierpont ME, Stewart FJ, Gorlin RJ.
    Am J Med Genet; 1998 Jan 06; 75(1):18-21. PubMed ID: 9450851
    [Abstract] [Full Text] [Related]

  • 10. Fronto-ocular syndrome: newly recognized trigonocephaly syndrome.
    Schneider EN, Bogdanow A, Goodrich JT, Marion RW, Cohen MM.
    Am J Med Genet; 2000 Jul 17; 93(2):89-93. PubMed ID: 10869108
    [Abstract] [Full Text] [Related]

  • 11. Orofaciodigital syndrome type-VI (Varadi-Papp syndrome) with several Y-shaped metacarpals.
    Mahato PR, Pandey SB.
    Indian J Hum Genet; 2012 Sep 17; 18(3):376-8. PubMed ID: 23716954
    [Abstract] [Full Text] [Related]

  • 12. [25 years' history of Váradi-Papp syndrome (orofaciodigital syndrome VI].
    Váradi V, Papp Z.
    Orv Hetil; 2005 Sep 25; 146(39):2017-22. PubMed ID: 16265870
    [Abstract] [Full Text] [Related]

  • 13. Multiple congenital anomalies/mental retardation syndrome with multiple circumferential skin creases: a new syndrome?
    Tinsa F, Aissa K, Meddeb M, Bousnina D, Boussetta K, Bousnina S.
    J Child Neurol; 2009 Feb 25; 24(2):224-7. PubMed ID: 19182162
    [Abstract] [Full Text] [Related]

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  • 17. Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation.
    Fryns JP.
    Am J Med Genet; 1996 Aug 23; 64(3):521-2. PubMed ID: 8862633
    [No Abstract] [Full Text] [Related]

  • 18. Provisional new syndrome of MR/MCA with evolving phenotype.
    Lacassie Y, Morava E, LaMotta I.
    Am J Med Genet; 2002 Nov 22; 113(2):213-7. PubMed ID: 12407715
    [Abstract] [Full Text] [Related]

  • 19. Trigonocephaly in rabbits with familial interfrontal suture synostosis: the multiple effects of premature single-suture fusion.
    Mooney MP, Cooper GM, Burrows AM, Wigginton W, Smith TD, Dechant J, Mitchell R, Losken HW, Siegel MI.
    Anat Rec; 2000 Nov 01; 260(3):238-51. PubMed ID: 11066035
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