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Journal Abstract Search

157 related items for PubMed ID: 5223982

  • 1. [On the causal and morphological etiology of the Pierre Robin syndrome].
    Becker R, Palm D.
    Dtsch Zahnarztl Z; 1966 Nov 01; 21(11):1321-38. PubMed ID: 5223982
    [No Abstract] [Full Text] [Related]

  • 2. [Genetic studies in Pierre Robin syndrome].
    Jörgensen G, Freund HJ.
    ZWR; 1979 Nov 10; 88(21):958-60. PubMed ID: 294009
    [No Abstract] [Full Text] [Related]

  • 3. Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.
    Melkoniemi M, Koillinen H, Männikkö M, Warman ML, Pihlajamaa T, Kääriäinen H, Rautio J, Hukki J, Stofko JA, Cisneros GJ, Krakow D, Cohn DH, Kere J, Ala-Kokko L.
    Eur J Hum Genet; 2003 Mar 10; 11(3):265-70. PubMed ID: 12673280
    [Abstract] [Full Text] [Related]

  • 4. [Syndromes 15. Robin sequence].
    Remmelink HJ, Bosschaart AN.
    Ned Tijdschr Tandheelkd; 1999 Oct 10; 106(10):369-72. PubMed ID: 11930430
    [Abstract] [Full Text] [Related]

  • 5. Stickler syndrome: report of four cases.
    Kulkarni ML, Sureshkumar C, George VG.
    Ann Dent; 1993 Oct 10; 52(2):23-7. PubMed ID: 8267375
    [No Abstract] [Full Text] [Related]

  • 6. Altered mandibular development precedes the time of palate closure in mice homozygous for disproportionate micromelia: an oral clefting model supporting the Pierre-Robin sequence.
    Ricks JE, Ryder VM, Bridgewater LC, Schaalje B, Seegmiller RE.
    Teratology; 2002 Mar 10; 65(3):116-20. PubMed ID: 11877774
    [Abstract] [Full Text] [Related]

  • 7. The genetic basis of the Pierre Robin Sequence.
    Jakobsen LP, Knudsen MA, Lespinasse J, García Ayuso C, Ramos C, Fryns JP, Bugge M, Tommerup N.
    Cleft Palate Craniofac J; 2006 Mar 10; 43(2):155-9. PubMed ID: 16526920
    [Abstract] [Full Text] [Related]

  • 8. [Robin Syndrome. Cleft palate, micrognathism and glossoptosis].
    Sandner O.
    Acta Odontol Venez; 1973 Mar 10; 11(2-3):283-94. PubMed ID: 4535358
    [No Abstract] [Full Text] [Related]

  • 9. [Synthesis of current knowledge on Pierre Robin syndrome].
    Dulude JA, Payette F.
    J Dent Que; 1991 Jan 10; 28():9-11. PubMed ID: 2056159
    [Abstract] [Full Text] [Related]

  • 10. A genetic follow-up study of 64 patients with the Pierre Robin complex.
    Sheffield LJ, Reiss JA, Strohm K, Gilding M.
    Am J Med Genet; 1987 Sep 10; 28(1):25-36. PubMed ID: 3674115
    [Abstract] [Full Text] [Related]

  • 11. Maxillonasal dysplasia, mandibular retrognathia and cleft palate.
    Mossey P, Sandham J.
    Angle Orthod; 1989 Sep 10; 59(4):257-61; discussion 262. PubMed ID: 2596747
    [Abstract] [Full Text] [Related]

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  • 14. Association of the Robin sequence with the fragile X syndrome.
    Lachiewicz AM, Hoegerman SF, Holmgren G, Holmberg E, Arinbjarnarson K.
    Am J Med Genet; 1991 Dec 01; 41(3):275-8. PubMed ID: 1789278
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  • 15. Variable expression of rib, pectus, and scapular anomalies with Robin-type cleft palate in a 5-generation family: a new syndrome?
    Stalker HJ, Zori RT.
    Am J Med Genet; 1997 Dec 19; 73(3):247-50. PubMed ID: 9415678
    [Abstract] [Full Text] [Related]

  • 16. [Congenital micrognathism, glossoptosis and fissure of the soft palate (Pierre Robin syndrome)].
    HERNANDEZ MT.
    Arch Argent Pediatr; 1961 Aug 19; 56():125-32. PubMed ID: 13906748
    [No Abstract] [Full Text] [Related]

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  • 19. What is 'Pierre Robin sequence'?
    Breugem CC, Mink van der Molen AB.
    J Plast Reconstr Aesthet Surg; 2009 Dec 19; 62(12):1555-8. PubMed ID: 18977702
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