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Journal Abstract Search

179 related items for PubMed ID: 7273460

  • 1. Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation.
    Silengo MC, Luzzatti L, Centerwall WR, Costello JM, Parslow M.
    Clin Genet; 1981 Mar; 19(3):174-80. PubMed ID: 7273460
    [Abstract] [Full Text] [Related]

  • 2. 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; 22(6):348-55. PubMed ID: 7160106
    [Abstract] [Full Text] [Related]

  • 3. Interstitial deletion of the short arm of chromosome 4.
    Ray M, Evans J, Rockman-Greenberg C, Wickstrom D.
    J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
    [Abstract] [Full Text] [Related]

  • 4. Interstitial deletion of the long arm of chromosome 5 in a boy with multiple congenital anomalies and mental retardation: Molecular characterization of the deleted region to 5q22.3q23.3.
    Garcia-Miñaur S, Ramsay J, Grace E, Minns RA, Myles LM, FitzPatrick DR.
    Am J Med Genet A; 2005 Feb 01; 132A(4):402-10. PubMed ID: 15742475
    [Abstract] [Full Text] [Related]

  • 5. Interstitial deletion of the long arm of chromosome 4 in a patient with mental retardation and abnormal phenotype.
    del Valle Torrado M, Labarta JD, Migliorini AM.
    J Med Genet; 1982 Dec 01; 19(6):477. PubMed ID: 6185682
    [No Abstract] [Full Text] [Related]

  • 6. Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution banding.
    de Die-Smulders CE, Engelen JJ, Albrechts JC, Hamers GJ.
    Am J Med Genet; 1999 Oct 08; 86(4):385-8. PubMed ID: 10494096
    [Abstract] [Full Text] [Related]

  • 7. Partial monosomy of long arm of chromosome 4 due to interstitial deletion.
    McDermott A, Cain R, Howell R.
    Hum Genet; 1980 Oct 08; 53(3):305-7. PubMed ID: 7372333
    [Abstract] [Full Text] [Related]

  • 8. Deletion of a portion of the long arm of chromosome 6.
    Goldberg R, Fish B, Ship A, Shprintzen RJ.
    Am J Med Genet; 1980 Oct 08; 5(1):73-80. PubMed ID: 7395903
    [Abstract] [Full Text] [Related]

  • 9. Interstitial deletion of chromosome 1 (q23-q25). Report of a case.
    Silengo MC, Davi GF, Bianco R, Biagioli M, Guala A, Franceschini P, Novelli G.
    Clin Genet; 1984 Jun 08; 25(6):549-52. PubMed ID: 6587954
    [Abstract] [Full Text] [Related]

  • 10. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).
    Stoll C, Levy J, Roth MP.
    J Med Genet; 1980 Dec 08; 17(6):486-7. PubMed ID: 7205434
    [Abstract] [Full Text] [Related]

  • 11. Interstitial deletion of the long arm of chromosome 18, del(18)(q12.2q21.1): a report of three cases of an autosomal deletion with a mild phenotype.
    Schinzel A, Binkert F, Lillington DM, Sands M, Stocks RJ, Lindenbaum RH, Matthews H, Sheridan H.
    J Med Genet; 1991 May 08; 28(5):352-5. PubMed ID: 1865477
    [Abstract] [Full Text] [Related]

  • 12. Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother.
    Tabor A, Andersen O, Lundsteen C, Niebuhr E, Sardemann H.
    Hum Genet; 1983 May 08; 64(2):196-9. PubMed ID: 6885061
    [Abstract] [Full Text] [Related]

  • 13. Terminal deletion 6p23: a case report.
    Kormann-Bortolotto MH, Farah LM, Soares D, Corbani M, Müller R, Adell AC.
    Am J Med Genet; 1990 Dec 08; 37(4):475-7. PubMed ID: 2260591
    [Abstract] [Full Text] [Related]

  • 14. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
    Zenger-Hain JL, Roberson J, Van Dyke DL, Weiss L.
    Am J Med Genet; 1993 Jun 01; 46(4):438-40. PubMed ID: 7689299
    [Abstract] [Full Text] [Related]

  • 15. Cat-like cry and mental retardation owing to 7q interstitial deletion (7q22 leads to 7q32).
    Abuelo DN, Padre-Mendoza T.
    J Med Genet; 1982 Dec 01; 19(6):473-6. PubMed ID: 7154049
    [Abstract] [Full Text] [Related]

  • 16. Molecular cytogenetic analysis of a de novo interstitial deletion of 5q23.3q31.2 and its phenotypic consequences.
    Tzschach A, Krause-Plonka I, Menzel C, Kalscheuer V, Toennies H, Scherthan H, Knoblauch A, Radke M, Ropers HH, Hoeltzenbein M.
    Am J Med Genet A; 2006 Mar 01; 140(5):496-502. PubMed ID: 16470790
    [Abstract] [Full Text] [Related]

  • 17. Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome.
    Yu CW, Chen H, Baucum RW, Hand AM.
    Ann Genet; 1981 Mar 01; 24(3):158-61. PubMed ID: 6974525
    [Abstract] [Full Text] [Related]

  • 18. Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant.
    Donahue ML, Ryan RM.
    Am J Med Genet; 1995 Mar 13; 56(1):97-100. PubMed ID: 7747796
    [Abstract] [Full Text] [Related]

  • 19. A unique de novo interstitial deletion del(17)(q21.3q23) in a phenotypically abnormal infant.
    Park JP, Moeschler JB, Berg SZ, Bauer RM, Wurster-Hill DH.
    Clin Genet; 1992 Jan 13; 41(1):54-6. PubMed ID: 1633649
    [Abstract] [Full Text] [Related]

  • 20. Interstitial de novo deletion of the long arm of chromosome 5: mapping of 5q bands associated with particular malformations.
    Rodewald A, Zankl M, Sitzmann FC, Zang KD.
    Clin Genet; 1982 Oct 13; 22(4):226-30. PubMed ID: 7151308
    [Abstract] [Full Text] [Related]

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