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Journal Abstract Search

143 related items for PubMed ID: 457139

  • 1. Terminal long-arm deletion of chromosome 1 in a male infant.
    Dignan PS, Soukup S.
    Hum Genet; 1979 Apr 27; 48(2):151-6. PubMed ID: 457139
    [Abstract] [Full Text] [Related]

  • 2. Terminal deletion of (1)(q42) and its phenotypical manifestations.
    Andrle M, Erlach A, Mayr WR, Rett A.
    Hum Genet; 1978 Feb 23; 41(1):115-20. PubMed ID: 631857
    [Abstract] [Full Text] [Related]

  • 3. Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43).
    Beemer FA, Klep-de Pater JM, Sepers GJ, Janssen B.
    Clin Genet; 1985 May 23; 27(5):515-9. PubMed ID: 4006278
    [Abstract] [Full Text] [Related]

  • 4. Two cases with different deletions of the long arm of chromosome 7.
    Klep-de Pater JM, Bijlsma JB, Bleeker-Wagemakers EM, de France HF, de Vries-Ekkers CM.
    J Med Genet; 1979 Apr 23; 16(2):151-4. PubMed ID: 458833
    [Abstract] [Full Text] [Related]

  • 5. Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
    Descartes M, Keppler-Noreuil K, Knops J, Longshore JW, Finley WH, Carroll AJ.
    Clin Genet; 1996 Dec 23; 50(6):538-40. PubMed ID: 9147894
    [Abstract] [Full Text] [Related]

  • 6. Terminal deletion with stable acentric fragment of 1q in a child with congenital malformations.
    Kucerová M, Polívková Z, Dluholucký S, Kvasnicová M.
    Am J Hum Genet; 1983 Jan 23; 35(1):91-5. PubMed ID: 6823976
    [Abstract] [Full Text] [Related]

  • 7. Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33.
    Tomkins DJ, Hunter AG, Uchida IA, Roberts MH.
    Clin Genet; 1982 Dec 23; 22(6):348-55. PubMed ID: 7160106
    [Abstract] [Full Text] [Related]

  • 8. Monosomy 1pter.
    Yunis E, Quintero L, Leibovici M.
    Hum Genet; 1981 Dec 23; 56(3):279-82. PubMed ID: 7239511
    [No Abstract] [Full Text] [Related]

  • 9. Partial monosomy of long arm of chromosome 4 due to interstitial deletion.
    McDermott A, Cain R, Howell R.
    Hum Genet; 1980 Dec 23; 53(3):305-7. PubMed ID: 7372333
    [Abstract] [Full Text] [Related]

  • 10. Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation.
    Franceschini P, Cirillo Silengo M, Davi G, Bianco R, Biagioli M.
    Hum Genet; 1983 Dec 23; 64(1):98. PubMed ID: 6873945
    [No Abstract] [Full Text] [Related]

  • 11. Partial deletion of the short arm of chromosome 3.
    Merrild U, Berggreen S, Hansen L, Mikkelsen M, Henningsen K.
    Eur J Pediatr; 1981 May 23; 136(2):211-6. PubMed ID: 7227394
    [Abstract] [Full Text] [Related]

  • 12. Terminal deletion of (1)(q42) in a newborn.
    Montero MR, Martinez A, Fayos JL, Alvarez V.
    Ann Genet; 1984 May 23; 27(3):178-9. PubMed ID: 6334483
    [No Abstract] [Full Text] [Related]

  • 13. Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomalies.
    Franceschini P, Cirillo Silengo M, Davi G, Bianco R, Biagioli M.
    Hum Genet; 1983 May 23; 64(1):97. PubMed ID: 6873944
    [No Abstract] [Full Text] [Related]

  • 14. A patient with a partial deletion of the short arm of chromosome 3.
    Verjaal M, De Nef MB.
    Am J Dis Child; 1978 Jan 23; 132(1):43-5. PubMed ID: 623063
    [Abstract] [Full Text] [Related]

  • 15. Partial trisomy for the short arm of chromosome 2 due to familial balance translocation.
    Sekhon GS, Taysi K, Rath R.
    Hum Genet; 1978 Oct 19; 44(1):99-103. PubMed ID: 711241
    [Abstract] [Full Text] [Related]

  • 16. Deletion of the short arm of chromosome 20.
    Vianna-Morgante AM, Richieri-Costa A, Rosenberg C.
    Clin Genet; 1987 Jun 19; 31(6):406-9. PubMed ID: 3621644
    [Abstract] [Full Text] [Related]

  • 17. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P, Vögtel D.
    Am J Med Genet; 1987 Oct 19; 28(2):371-6. PubMed ID: 3322005
    [Abstract] [Full Text] [Related]

  • 18. Trigonocephaly and the Opitz C syndrome.
    Sargent C, Burn J, Baraitser M, Pembrey ME.
    J Med Genet; 1985 Feb 19; 22(1):39-45. PubMed ID: 3981579
    [Abstract] [Full Text] [Related]

  • 19. Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-->q27).
    Vermeesch JR, Fryns JP.
    Am J Med Genet A; 2003 Jul 15; 120A(2):299-300. PubMed ID: 12833421
    [No Abstract] [Full Text] [Related]

  • 20. Developmental abnormalities associated with long arm deletion of chromosome No. 6.
    Bartoshesky L, Lewis MB, Pashayan HM.
    Clin Genet; 1978 Jan 15; 13(1):68-71. PubMed ID: 624189
    [Abstract] [Full Text] [Related]

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