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Journal Abstract Search

321 related items for PubMed ID: 6587954

  • 1. 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; 25(6):549-52. PubMed ID: 6587954
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Interstitial deletion in the long arms of chromosome 1: 46,XY,del(1)(pter leads to q22::q25 leads to qter).
    de Pablo CE, García Sagredo JM, Ferro MT, Ferrando P, San Román C.
    J Med Genet; 1980 Dec; 17(6):483-6. PubMed ID: 6937620
    [Abstract] [Full Text] [Related]

  • 4. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
    Taysi K, Dengler DR, Jones LA, Heersma JR.
    Ann Genet; 1981 Dec; 24(4):245-7. PubMed ID: 7036843
    [No Abstract] [Full Text] [Related]

  • 5. Duplication 3q: severe manifestations in an infant with duplication of a short segment of 3q.
    Rosenfeld W, Verma RS, Jhaveri RC, Estrada R, Evans H, Dosik H.
    Am J Med Genet; 1981 Dec; 10(2):187-92. PubMed ID: 7315875
    [Abstract] [Full Text] [Related]

  • 6. De novo interstitial deletion del(1)(p21p32).
    Bene M, Duca-Marinescu A, Ioan D, Maximilian C.
    J Med Genet; 1979 Aug; 16(4):323-7. PubMed ID: 490590
    [Abstract] [Full Text] [Related]

  • 7. 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; 17(6):486-7. PubMed ID: 7205434
    [Abstract] [Full Text] [Related]

  • 8. 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 Dec; 64(1):97. PubMed ID: 6873944
    [No Abstract] [Full Text] [Related]

  • 9. Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies.
    Elejalde BR, Opitz JM, de Elejalde MM, Gilbert EF, Abellera M, Meisner L, Lebel RR, Hartigan JM.
    Am J Med Genet; 1984 Apr; 17(4):723-30. PubMed ID: 6539070
    [Abstract] [Full Text] [Related]

  • 10. 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; 27(5):515-9. PubMed ID: 4006278
    [Abstract] [Full Text] [Related]

  • 11. 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; 41(1):54-6. PubMed ID: 1633649
    [Abstract] [Full Text] [Related]

  • 12. Chromosome 7 short arm deletion, 7p21----pter.
    Schömig-Spingler M, Schmid M, Brosi W, Grimm T.
    Hum Genet; 1986 Nov; 74(3):323-5. PubMed ID: 3781561
    [Abstract] [Full Text] [Related]

  • 13. 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; 50(6):538-40. PubMed ID: 9147894
    [Abstract] [Full Text] [Related]

  • 14. A girl with an interstitial deletion of the short arm of chromosome 3 studied with a high-resolution banding technique.
    Sichong Z, Bui TH, Castro I, Iselius L, Håkansson S, Lundmark KM.
    Hum Genet; 1981 Dec; 59(2):178-81. PubMed ID: 7327578
    [Abstract] [Full Text] [Related]

  • 15. 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; 64(1):98. PubMed ID: 6873945
    [No Abstract] [Full Text] [Related]

  • 16. Chromosome 22q11 deletion and other chromosome aberrations in cases with cleft palate, congenital heart defects and/or mental disability. A survey based on the Danish Facial Cleft Register.
    Brøndum-Nielsen K, Christensen K.
    Clin Genet; 1996 Sep; 50(3):116-20. PubMed ID: 8946108
    [Abstract] [Full Text] [Related]

  • 17. Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literature.
    Fryns JP, Kleczkowska A, Van den Berghe H.
    Ann Genet; 1990 Sep; 33(1):43-5. PubMed ID: 2195980
    [Abstract] [Full Text] [Related]

  • 18. Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review.
    Stockton DW, Ross HL, Bacino CA, Altman CA, Shaffer LG, Lupski JR.
    Am J Med Genet; 1997 Aug 08; 71(2):189-93. PubMed ID: 9217220
    [Abstract] [Full Text] [Related]

  • 19. Proximal deletion of the long arm of chromosome 1: [del(1)(q23-q25)].
    Lo LJ, Noordhoff MS, Huang CS, Chen KT, Chen YR.
    Cleft Palate Craniofac J; 1993 Nov 08; 30(6):586-9. PubMed ID: 8280739
    [Abstract] [Full Text] [Related]

  • 20. De novo translocation involving chromosomes 2, 8, and 20.
    Zaletajev DV, Marincheva GS, Tsvetkova TG.
    J Med Genet; 1984 Jun 08; 21(3):231. PubMed ID: 6748024
    [No Abstract] [Full Text] [Related]

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