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Journal Abstract Search

710 related items for PubMed ID: 7985983

  • 1. Isochromosome-formation in chromosome 9.
    Miller K, Arslan-Kirchner M.
    Ann Genet; 1994; 37(2):78-81. PubMed ID: 7985983
    [Abstract] [Full Text] [Related]

  • 2. Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.
    Lindgren V, Rosinsky B, Chin J, Berry-Kravis E.
    Am J Med Genet; 1994 Jan 01; 49(1):67-73. PubMed ID: 8172253
    [Abstract] [Full Text] [Related]

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  • 4. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
    Mewar R, Harrison W, Weaver DD, Palmer C, Davee MA, Overhauser J.
    Am J Med Genet; 1994 Aug 15; 52(2):178-83. PubMed ID: 7802005
    [Abstract] [Full Text] [Related]

  • 5. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J, Kimijima Y, Yamada S, Amagasa T, Saito-Ohara F.
    J Craniomaxillofac Surg; 2000 Jun 15; 28(3):165-70. PubMed ID: 10964553
    [Abstract] [Full Text] [Related]

  • 6. Chromosomal mosaicism in the Killian/Teschler-Nicola syndrome.
    Raffel LJ, Mohandas T, Rimoin DL.
    Am J Med Genet; 1986 Aug 15; 24(4):607-11. PubMed ID: 3740095
    [Abstract] [Full Text] [Related]

  • 7. De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girl.
    Jenkins EC, Curcuru-Giordano FM, Krishna SG, Cantarella J.
    Ann Genet; 1975 Jun 15; 18(2):117-20. PubMed ID: 1081364
    [Abstract] [Full Text] [Related]

  • 8. Distal monosomy of the long arm of chromosome 6 (6q25----6qter) inherited by maternal translocation t(6q;17q).
    Oliveira-Duarte MH, Martelli-Soares LR, Sarquis-Cintra T, Machado ML, Lison MP.
    Ann Genet; 1990 Jun 15; 33(1):56-9. PubMed ID: 2195984
    [Abstract] [Full Text] [Related]

  • 9. [The clinical picture of 13q22-qter duplication in a 2-year-old boy].
    Halasová E, Lukácová M, Bergendiová E, Kamenická E.
    Cesk Pediatr; 1987 Aug 15; 42(8):477-9. PubMed ID: 3664759
    [No Abstract] [Full Text] [Related]

  • 10. Interstitial deletion of chromosome 2 (p23p25).
    Penchaszadeh VB, Dowling PK, Davis JG, Schmidt R, Wapnir RA.
    Am J Med Genet; 1987 Jul 15; 27(3):701-6. PubMed ID: 3477099
    [Abstract] [Full Text] [Related]

  • 11. Duplication 10q confirmed by DNA in situ hybridization.
    Johnson VP, Sutliff WC.
    Am J Med Genet; 1994 Aug 15; 52(2):184-7. PubMed ID: 7802006
    [Abstract] [Full Text] [Related]

  • 12. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
    Frankova YE, Holenova H, Braulke I.
    Monatsschr Kinderheilkd; 1991 Dec 15; 139(12):841-3. PubMed ID: 1770961
    [Abstract] [Full Text] [Related]

  • 13. Mosaic isochromosome 8p.
    Tilstra DJ, Grove M, Spencer AC, Norwood TH, Pagon RA.
    Am J Med Genet; 1993 Jun 15; 46(5):517-9. PubMed ID: 8322812
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  • 15. Deletion of 2p: a cytogenetic and clinical update.
    Neidich J, Zackai E, Aronson M, Emanuel BS.
    Am J Med Genet; 1987 Jul 15; 27(3):707-10. PubMed ID: 3477100
    [Abstract] [Full Text] [Related]

  • 16. Ring chromosome 7 in an Indian woman.
    Kaur A, Dhillon S, Garg PD, Singh JR.
    J Intellect Dev Disabil; 2008 Mar 15; 33(1):87-94. PubMed ID: 18300171
    [Abstract] [Full Text] [Related]

  • 17. Familial partial duplication (1)(p21p31).
    Hoechstetter L, Soukup S, Schorry EK.
    Am J Med Genet; 1995 Nov 20; 59(3):291-4. PubMed ID: 8599351
    [Abstract] [Full Text] [Related]

  • 18. Ring chromosome 5 associated with severe growth retardation as the sole major physical abnormality.
    Migliori MV, Cherubini V, Bartolotta E, Pettinari A, Pecora R.
    Am J Med Genet; 1994 Jan 01; 49(1):108-10. PubMed ID: 8172236
    [Abstract] [Full Text] [Related]

  • 19. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
    de Die-Smulders CE, Engelen JJ, Schrander-Stumpel CT, Govaerts LC, de Vries B, Vles JS, Wagemans A, Schijns-Fleuren S, Gillessen-Kaesbach G, Fryns JP.
    Am J Med Genet; 1995 Nov 20; 59(3):369-74. PubMed ID: 8599364
    [Abstract] [Full Text] [Related]

  • 20. Trisomy 9 mosaicism in a girl with multiple malformations.
    Diaz-Mares L, Molina B, Carnevale A.
    Ann Genet; 1990 Nov 20; 33(3):165-8. PubMed ID: 2288462
    [Abstract] [Full Text] [Related]

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