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Journal Abstract Search

171 related items for PubMed ID: 9677069

  • 1. Interstitial deletion of the long arm of chromosome 4 [del(4)(q21.22q23)] and a liver tumor.
    Suwa K, Momoi MY, Yamagata T, Mori Y.
    Am J Med Genet; 1998 Jul 07; 78(3):291-3. PubMed ID: 9677069
    [Abstract] [Full Text] [Related]

  • 2. Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?
    Rauen KA, Albertson DG, Pinkel D, Cotter PD.
    Am J Med Genet; 2002 Jun 01; 110(1):51-6. PubMed ID: 12116271
    [Abstract] [Full Text] [Related]

  • 3. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
    Copelli S, del Rey G, Heinrich J, Coco R.
    Am J Med Genet; 1995 Jan 02; 55(1):77-9. PubMed ID: 7702102
    [Abstract] [Full Text] [Related]

  • 4. Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype.
    Velinov M, Kupferman J, Gu H, Macera MJ, Babu A, Jenkins EC, Kupchik G.
    Eur J Med Genet; 2005 Jan 02; 48(1):51-5. PubMed ID: 15953406
    [Abstract] [Full Text] [Related]

  • 5. Infantile hemangioendothelioma of the liver in patient with interstitial deletion of chromosome 6q: report of an autopsy case.
    Ito H, Yamasaki T, Okamoto O, Tahara E.
    Am J Med Genet; 1989 Nov 02; 34(3):325-9. PubMed ID: 2596522
    [Abstract] [Full Text] [Related]

  • 6. Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly.
    Kulharya AS, Maberry M, Kukolich MK, Day DW, Schneider NR, Wilson GN, Tonk V.
    Am J Med Genet; 1995 Jan 16; 55(2):165-70. PubMed ID: 7717415
    [Abstract] [Full Text] [Related]

  • 7. An 8-cM interstitial deletion on 4q21-q22 in DNA from an infant with hepatoblastoma overlaps with a commonly deleted region in adult liver cancers.
    Terada Y, Imoto I, Nagai H, Suwa K, Momoi M, Tajiri T, Onda M, Inazawa J, Emi M.
    Am J Med Genet; 2001 Oct 01; 103(2):176-80. PubMed ID: 11568928
    [Abstract] [Full Text] [Related]

  • 8. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S, Wang S, Hoang K, Vanchiere CM, England K, Fick R, Pagon B, Reddy KS.
    Am J Med Genet; 1999 Nov 05; 87(1):17-22. PubMed ID: 10528241
    [Abstract] [Full Text] [Related]

  • 9. [Del(1)(q22-q25) syndrome. Cytogenetics and phenotype].
    Zaletaev DV, Dadali EL, Kuleshov NP.
    Tsitol Genet; 1987 Nov 05; 21(3):213-6. PubMed ID: 3617217
    [Abstract] [Full Text] [Related]

  • 10. 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 Nov 05; 24(3):158-61. PubMed ID: 6974525
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4.
    Beall MH, Falk RE, Ying KL.
    Am J Med Genet; 1988 Nov 01; 31(3):553-7. PubMed ID: 3067576
    [Abstract] [Full Text] [Related]

  • 13. A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2.
    Ramer JC, Ladda RL, Frankel CA, Beckford A.
    Am J Med Genet; 1989 Mar 01; 32(3):359-63. PubMed ID: 2658585
    [Abstract] [Full Text] [Related]

  • 14. 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 Mar 01; 51(1):61-7. PubMed ID: 17998173
    [Abstract] [Full Text] [Related]

  • 15. Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newborns.
    Fryns JP, Kleczkowska A, Limbos C, Vandecasseye W, Van den Berghe H.
    Ann Genet; 1985 Mar 01; 28(4):248-50. PubMed ID: 3879440
    [Abstract] [Full Text] [Related]

  • 16. Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37).
    Wang TH, Johnston K, Hsieh CL, Dennery PA.
    Am J Med Genet; 1994 Feb 15; 49(4):399-401. PubMed ID: 8160733
    [Abstract] [Full Text] [Related]

  • 17. Holoprosencephaly, ear abnormalities, congenital heart defect, and microphallus in a patient with 11q- mosaicism.
    Helmuth RA, Weaver DD, Wills ER.
    Am J Med Genet; 1989 Feb 15; 32(2):178-81. PubMed ID: 2494886
    [Abstract] [Full Text] [Related]

  • 18. The 4q-Syndrome.
    Strehle EM, Ahmed OA, Hameed M, Russell A.
    Genet Couns; 2001 Feb 15; 12(4):327-39. PubMed ID: 11837601
    [Abstract] [Full Text] [Related]

  • 19. Proximal interstitial deletion of 7q: a case report and review of the literature.
    Zackowski JL, Raffel LJ, Blank CA, Schwartz S.
    Am J Med Genet; 1990 Jul 15; 36(3):328-32. PubMed ID: 2194394
    [Abstract] [Full Text] [Related]

  • 20. Deletion 4q21/4q22 syndrome: two patients with de novo 4q21.3q23 and 4q13.2q23 deletions.
    Nowaczyk MJ, Teshima IE, Siegel-Bartelt J, Clarke JT.
    Am J Med Genet; 1997 Apr 14; 69(4):400-5. PubMed ID: 9098490
    [Abstract] [Full Text] [Related]

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