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Journal Abstract Search

92 related items for PubMed ID: 6748329

  • 1. A case of an interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q15q22).
    Fukuda T, Fukushima Y, Kuroki Y.
    Jinrui Idengaku Zasshi; 1984 Mar; 29(1):63-7. PubMed ID: 6748329
    [No Abstract] [Full Text] [Related]

  • 2. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
    Young RS, Palmer CG, Bender HA, Weaver DD, Hodes ME.
    Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
    [No Abstract] [Full Text] [Related]

  • 3. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
    Wilson MG, Towner JW, Forsman I, Siris E.
    Am J Med Genet; 1979 May; 3(2):155-74. PubMed ID: 474629
    [Abstract] [Full Text] [Related]

  • 4. Brief clinical report: interstitial deletion of the long arm of chromosome 10: del(10)(q11.2q21).
    Holden JJ, MacDonald EA.
    Am J Med Genet; 1985 Feb; 20(2):245-8. PubMed ID: 2579554
    [Abstract] [Full Text] [Related]

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  • 7. Interstitial deletion of the long arm of chromosome 2: a case report and review of the literature.
    Takahashi Y, Narahara K, Kikkawa K, Wakita Y, Kimura S, Murakami M, Kasai R, Kimoto H.
    Jinrui Idengaku Zasshi; 1985 Dec; 30(4):297-305. PubMed ID: 3869838
    [No Abstract] [Full Text] [Related]

  • 8. Deletions of the long arm of chromosome 10.
    Shapiro SD, Hansen KL, Pasztor LM, DiLiberti JH, Jorgenson RJ, Young RS, Moore CM.
    Am J Med Genet; 1985 Jan; 20(1):181-96. PubMed ID: 3970071
    [Abstract] [Full Text] [Related]

  • 9. Partial monosomy for chromosome 22 in a girl with mental retardation.
    Yong YP, Knight LA, Yong MH, Lam S, Ho LY.
    Singapore Med J; 1997 Feb; 38(2):85-6. PubMed ID: 9269370
    [Abstract] [Full Text] [Related]

  • 10. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
    Mdzin R, Ko C, Abdul Latif Z, Zakaria Z.
    Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
    [Abstract] [Full Text] [Related]

  • 11. Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases.
    Poissonnier M, Turleau C, Olivier-Martin M, Milleret-Proyart MJ, Prieur M, Dubos M, Cabanis MO, Mugneret F, Blanc P, Noel L.
    Ann Genet; 1992 Nov; 35(3):146-51. PubMed ID: 1466563
    [Abstract] [Full Text] [Related]

  • 12. Long arm deletion of chromosome no. 6 in a mentally retarded boy with multiple physical malformations.
    Milosević J, Kalicanin P.
    J Ment Defic Res; 1975 Jun; 19(2):139-44. PubMed ID: 1195357
    [Abstract] [Full Text] [Related]

  • 13. Interstitial deletion and ring chromosome derived from 19q. Proximal 19q trisomy phenotype.
    Quack B, Van Roy N, Verschraegen-Spae MR, Klein F.
    Ann Genet; 1992 Jun; 35(4):241-4. PubMed ID: 1296524
    [Abstract] [Full Text] [Related]

  • 14. Interstitial deletion of long arm of chromosome 13.
    Carnevale A, Frias S, Alcantar R.
    Ann Genet; 1984 Jun; 27(1):49-52. PubMed ID: 6609673
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Long arm deletion of chromosome 13 with exclusion of esterase D from 13q32 leads to 13qter.
    Telfer MA, Clark CE, Casey PA, Cowell HR, Stroud HH.
    Clin Genet; 1980 Jun 02; 17(6):428-32. PubMed ID: 7398115
    [Abstract] [Full Text] [Related]

  • 17. Terminal deletion of long arm of chromosome 4: patient report and literature review.
    Evers LJ, Schrander-Stumpel CT, Engelen JJ, Mulder H, Borghgraef M, Fryns JP.
    Genet Couns; 1993 Jun 02; 4(2):139-45. PubMed ID: 7689326
    [Abstract] [Full Text] [Related]

  • 18. Interstitial deletion of the short arm of chromosome 8: report of a patient and review of the literature.
    Plomp AS, Schrander-Stumpel CT, Engelen JJ, Sijstermans JM, Loneus WH, Fryns JP.
    Genet Couns; 1995 Jun 02; 6(1):55-60. PubMed ID: 7794563
    [Abstract] [Full Text] [Related]

  • 19. Blepharophimosis sequence (BPES) and microcephaly in a girl with del(3) (q22.2q23): a putative gene responsible for microcephaly close to the BPES gene?
    Ishikiriyama S, Goto M.
    Am J Med Genet; 1993 Sep 15; 47(4):487-9. PubMed ID: 8256811
    [Abstract] [Full Text] [Related]

  • 20. Langer-Giedion syndrome with interstitial 8q-deletion.
    Zabel BU, Baumann WA.
    Am J Med Genet; 1982 Mar 15; 11(3):353-8. PubMed ID: 7081298
    [Abstract] [Full Text] [Related]

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