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Journal Abstract Search

92 related items for PubMed ID: 3499845

  • 1. Terminal deletion 1q43 in a newborn with hydrocephalus.
    Ribeiro MC, Brunoni D.
    Ann Genet; 1987; 30(2):126-8. PubMed ID: 3499845
    [Abstract] [Full Text] [Related]

  • 2. Deletion of the distal long arm of chromosome 1: a definable syndrome.
    Johnson VP, Heck LJ, Carter GA, Flom JO.
    Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
    [Abstract] [Full Text] [Related]

  • 3. Deletion 5q35.3.
    Stratton RF, Tedrowe NA, Tolworthy JA, Patterson RM, Ryan SG, Young RS.
    Am J Med Genet; 1994 Jun 01; 51(2):150-2. PubMed ID: 8092192
    [Abstract] [Full Text] [Related]

  • 4. Interstitial deletion of the long arm of chromosome 11: report of a case and review of the literature.
    Wakazono A, Masuno M, Yamaguchi S, Tsubouchi K, Kondo N, Orii T.
    Jpn J Hum Genet; 1992 Sep 01; 37(3):229-34. PubMed ID: 1472705
    [Abstract] [Full Text] [Related]

  • 5. Distal 11q deletion: a specific clinical entity.
    Fryns JP, Kleczkowska A, Smeets E, Van den Berghe H.
    Helv Paediatr Acta; 1987 Oct 01; 42(2-3):191-4. PubMed ID: 3692885
    [Abstract] [Full Text] [Related]

  • 6. [Distal 1q monosomy. 2 new cases and description of the syndrome].
    Turleau C, de Grouchy J, Frézal J, Richardet JM.
    Ann Genet; 1983 Oct 01; 26(3):161-4. PubMed ID: 6606378
    [Abstract] [Full Text] [Related]

  • 7.
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    [No Abstract] [Full Text] [Related]

  • 8. [Del(1)(q22-q25) syndrome. Cytogenetics and phenotype].
    Zaletaev DV, Dadali EL, Kuleshov NP.
    Tsitol Genet; 1987 Oct 01; 21(3):213-6. PubMed ID: 3617217
    [Abstract] [Full Text] [Related]

  • 9. [Syndrome of terminal deletion of the long arm of chromosome 4. Apropos of a personal case with a review of the literature].
    Frappaz D, Bourgeois J, Berthier JC, Laurent C, Bethenod M.
    Pediatrie; 1983 Jun 01; 38(4):261-70. PubMed ID: 6353348
    [Abstract] [Full Text] [Related]

  • 10. Further delineation of the chromosome 14q terminal deletion syndrome.
    van Karnebeek CD, Quik S, Sluijter S, Hulsbeek MM, Hoovers JM, Hennekam RC.
    Am J Med Genet; 2002 Jun 01; 110(1):65-72. PubMed ID: 12116274
    [Abstract] [Full Text] [Related]

  • 11. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.
    Taysi K, Strauss AW, Yang V, Padmalatha C, Marshall RE.
    Ann Genet; 1982 Jun 01; 25(3):141-4. PubMed ID: 6982660
    [Abstract] [Full Text] [Related]

  • 12. Distal del(4) (q33) syndrome: detailed clinical presentation and molecular description with array-CGH.
    Kitsiou-Tzeli S, Sismani C, Koumbaris G, Ioannides M, Kanavakis E, Kolialexi A, Mavrou A, Touliatou V, Patsalis PC.
    Eur J Med Genet; 2008 Jun 01; 51(1):61-7. PubMed ID: 17998173
    [Abstract] [Full Text] [Related]

  • 13. A terminal long arm deletion of chromosome 16 in a dysmorphic infant: 46,XY,del(16) (q22).
    Taysi K, Fishman M, Sekhon GS.
    Birth Defects Orig Artic Ser; 1978 Jun 01; 14(6C):343-7. PubMed ID: 728588
    [No Abstract] [Full Text] [Related]

  • 14. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
    Mégarbané A, Souraty N, Theophile D, Vekemans M, Samaras L, Ghorayeb Z.
    Ann Genet; 1997 Jun 01; 40(1):55-9. PubMed ID: 9150851
    [Abstract] [Full Text] [Related]

  • 15. Dup(1q)(q42-->qter) syndrome: case report and review of literature.
    Kennerknecht I, Barbi G, Rodens K.
    Am J Med Genet; 1993 Dec 01; 47(8):1157-60. PubMed ID: 7507296
    [Abstract] [Full Text] [Related]

  • 16. Terminal deletion of 6p: report of a new case.
    Plaja A, Vidal R, Soriano D, Bou X, Vendrell T, Mediano C, Pueyo JM, Labraña X, Sarret E.
    Ann Genet; 1994 Dec 01; 37(4):196-9. PubMed ID: 7710255
    [Abstract] [Full Text] [Related]

  • 17. Chromosome 13 long arm interstitial deletion associated with features of Noonan phenotype.
    Onufer CN, Stephan MJ, Thuline HC, Char F.
    Ann Genet; 1987 Dec 01; 30(4):236-9. PubMed ID: 3501267
    [Abstract] [Full Text] [Related]

  • 18. Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)].
    Al-Awadi SA, Farag TI, Usha R, el-Khalifa MY, Sundareshan TS, Al-Othman SA.
    Am J Med Genet; 1986 Apr 01; 23(4):931-3. PubMed ID: 3963055
    [Abstract] [Full Text] [Related]

  • 19. Toriello-Carey syndrome in a Turkish newborn.
    Uras N, Sandal G, Oguz S, Aydemir O, Erdeve O, Dilmen U.
    Genet Couns; 2009 Apr 01; 20(3):243-7. PubMed ID: 19852430
    [Abstract] [Full Text] [Related]

  • 20. Deletions of different segments of the long arm of chromosome 4.
    Mitchell JA, Packman S, Loughman WD, Fineman RM, Zackai E, Patil SR, Emanual B, Bartley JA, Hanson JW.
    Am J Med Genet; 1981 Apr 01; 8(1):73-89. PubMed ID: 7246608
    [Abstract] [Full Text] [Related]

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