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PUBMED FOR HANDHELDS

Journal Abstract Search

257 related items for PubMed ID: 8267000

  • 1. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients.
    Richieri-Costa A, Pereira SC.
    Am J Med Genet; 1993 Oct 01; 47(5):707-9. PubMed ID: 8267000
    [Abstract] [Full Text] [Related]

  • 2. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome.
    Richieri-Costa A, Pereira SC.
    Am J Med Genet; 1992 Mar 01; 42(5):681-7. PubMed ID: 1632438
    [Abstract] [Full Text] [Related]

  • 3. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected Brazilian patient born to consanguineous parents.
    Richieri-Costa A, Brandão-Almeida IL.
    Am J Med Genet; 1997 Aug 08; 71(2):233-5. PubMed ID: 9217230
    [No Abstract] [Full Text] [Related]

  • 4. The Richieri-Costa and Pereira form of acrofacial dysostosis: first case in a non-Brazilian infant.
    Walter-Nicolet E, Coëslier A, Joriot S, Kacet N, Moerman A, Manouvrier-Hanu S.
    Am J Med Genet; 1999 Dec 22; 87(5):430-3. PubMed ID: 10594883
    [Abstract] [Full Text] [Related]

  • 5. Catel-Manzke syndrome: two new patients and a critical review of the literature.
    Manzke H, Lehmann K, Klopocki E, Caliebe A.
    Eur J Med Genet; 2008 Dec 22; 51(5):452-65. PubMed ID: 18501694
    [Abstract] [Full Text] [Related]

  • 6. Syndrome of cleft palate, microcephaly, large ears, and short stature (Say syndrome).
    Abu-Libdeh B, Fujimoto A, Ehinger M.
    Am J Med Genet; 1993 Feb 01; 45(3):358-60. PubMed ID: 8434624
    [Abstract] [Full Text] [Related]

  • 7. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family.
    Richieri-Costa A, Guion-Almeida ML, Pagnan NA.
    Am J Med Genet; 1992 Dec 01; 44(6):800-2. PubMed ID: 1481850
    [Abstract] [Full Text] [Related]

  • 8. Richieri-Costa-Pereira syndrome: a unique acrofacial dysostosis type. An overview of the Brazilian cases.
    Favaro FP, Zechi-Ceide RM, Alvarez CW, Maximino LP, Antunes LF, Richieri-Costa A, Guion-Almeida ML.
    Am J Med Genet A; 2011 Feb 01; 155A(2):322-31. PubMed ID: 21271648
    [Abstract] [Full Text] [Related]

  • 9. A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs.
    Schinzel A, Giedion A.
    Am J Med Genet; 1978 Feb 01; 1(4):361-75. PubMed ID: 665725
    [Abstract] [Full Text] [Related]

  • 10. Catel-Manzke syndrome: a clinical report suggesting autosomal recessive inheritance.
    Kiper PÖ, Utine GE, Boduroğlu K, Alanay Y.
    Am J Med Genet A; 2011 Sep 01; 155A(9):2288-92. PubMed ID: 21834032
    [Abstract] [Full Text] [Related]

  • 11. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.
    Saal HM, Greenstein RM, Weinbaum PJ, Poole AE.
    Am J Med Genet; 1988 Jul 01; 30(3):709-18. PubMed ID: 3189394
    [Abstract] [Full Text] [Related]

  • 12. Robin sequence with facial and digital anomalies in two half-brothers by the same mother.
    Chitayat D, Meunier CM, Hodgkinson KA, Azouz ME.
    Am J Med Genet; 1991 Aug 01; 40(2):167-72. PubMed ID: 1897570
    [Abstract] [Full Text] [Related]

  • 13. Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome.
    Ferreira de Lima RL, Moretti-Ferreira D, Richieri-Costa A, Murray JC.
    Am J Med Genet A; 2003 Sep 15; 122A(1):56-8. PubMed ID: 12949973
    [Abstract] [Full Text] [Related]

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  • 15. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G, Centa A, Pozzolo S, Camera A.
    Clin Dysmorphol; 1993 Oct 15; 2(4):317-21. PubMed ID: 8305962
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  • 18. Further evidence for genetic heterogeneity of whistling face or Freeman-Sheldon syndrome in a Chinese family.
    Wang TR, Lin SJ.
    Am J Med Genet; 1987 Oct 15; 28(2):471-5. PubMed ID: 3425620
    [Abstract] [Full Text] [Related]

  • 19. Auditory canal atresia, humeroscapular synostosis, and other skeletal abnormalities: confirmation of the autosomal recessive "SAMS" syndrome.
    ter Heide H, Bulstra SK, Reekers A, Schrander JJ, Schrander-Stumpel CT.
    Am J Med Genet; 2002 Jul 15; 110(4):359-64. PubMed ID: 12116210
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