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Journal Abstract Search

356 related items for PubMed ID: 8469652

  • 1. [Genetic morphological fatal syndromes. The Fryns syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar; 14(2):92-3. PubMed ID: 8469652
    [No Abstract] [Full Text] [Related]

  • 2. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar; 14(2):91-2. PubMed ID: 8469651
    [No Abstract] [Full Text] [Related]

  • 3. [Genetic morphological fatal syndromes. The cryptophthalmos syndrome (Fraser syndrome)].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar; 14(2):94-5. PubMed ID: 8469653
    [No Abstract] [Full Text] [Related]

  • 4. Antley-Bixler syndrome: case report and review of the literature.
    Poddevin F, Delobel B, Courreges P, Bayart M.
    Genet Couns; 1995 Mar; 6(3):241-6. PubMed ID: 8588853
    [Abstract] [Full Text] [Related]

  • 5. [Fryns syndrome: report of the first case in the national literature].
    Rentería-Ibarra M, Frías-Márquez SG, Michel-Aceves RJ, Navarrete-Arellano M.
    Bol Med Hosp Infant Mex; 1993 Sep; 50(9):666-70. PubMed ID: 8373549
    [Abstract] [Full Text] [Related]

  • 6. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.
    Cunniff C, Jones KL, Saal HM, Stern HJ.
    Pediatrics; 1990 Apr; 85(4):499-504. PubMed ID: 2314962
    [Abstract] [Full Text] [Related]

  • 7. Fryns syndrome without diaphragmatic hernia. Report on a new case and review of the literature.
    Alessandri L, Brayer C, Attali T, Samperiz S, Tiran-Rajaofera I, Ramful D, Pilorget H.
    Genet Couns; 2005 Apr; 16(4):363-70. PubMed ID: 16440878
    [Abstract] [Full Text] [Related]

  • 8. Pallister-Killian and Fryns syndromes.
    Stratton RF, Moore CM, Popham CS, DuPont BR, Mattern VL.
    Am J Med Genet; 1994 May 15; 51(1):90. PubMed ID: 8030681
    [No Abstract] [Full Text] [Related]

  • 9. [Fatal genetic-morphologic syndromes. The campomelic syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 May 15; 14(3):162-4. PubMed ID: 8516273
    [No Abstract] [Full Text] [Related]

  • 10. "C" trigonocephaly syndrome with diaphragmnatic hernia.
    Addor MC, Stefanutti D, Farron F, Meinecke P, Lacombe D, Sarlangue J, Prescia G, Schorderet DF.
    Genet Couns; 1995 May 15; 6(2):113-20. PubMed ID: 7546453
    [Abstract] [Full Text] [Related]

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  • 14. Pallister-Killian and Fryns syndromes: nosology.
    McPherson EW, Ketterer DM, Salsburey DJ.
    Am J Med Genet; 1993 Aug 15; 47(2):241-5. PubMed ID: 8213912
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  • 17. Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome.
    Goddeeris P, Fryns JP, van den Berghe H.
    J Genet Hum; 1980 Mar 15; 28(1):57-60. PubMed ID: 7400786
    [Abstract] [Full Text] [Related]

  • 18. "Isolated" radial ray defect may be due to Rothmund-Thomson syndrome.
    Moss C, Bacon CJ, Mueller RF.
    Clin Genet; 1990 Oct 15; 38(4):318-9. PubMed ID: 2268978
    [No Abstract] [Full Text] [Related]

  • 19. Further delineation of the Yunis-Varon syndrome.
    Hennekam RC, Vermeulen-Meiners C.
    J Med Genet; 1989 Jan 15; 26(1):55-8. PubMed ID: 2918527
    [Abstract] [Full Text] [Related]

  • 20. Fryns syndrome without diaphragmatic hernia?
    Willems PJ, Keersmaekers GH, Dom KE, Colpaert C, Schatteman E, Vergote IB, Dumon JE.
    Am J Med Genet; 1991 Nov 01; 41(2):255-7. PubMed ID: 1785645
    [Abstract] [Full Text] [Related]

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