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Journal Abstract Search

156 related items for PubMed ID: 3901750

  • 1. Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.
    Dobyns WB, Dewald GW, Carlson RO, Mair DD, Michels VV.
    Am J Med Genet; 1985 Sep; 22(1):125-34. PubMed ID: 3901750
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  • 2. 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 Sep; 24(4):245-7. PubMed ID: 7036843
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  • 6. Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.
    Narahara K, Kikkawa K, Murakami M, Hiramoto K, Namba H, Tsuji K, Yokoyama Y, Kimoto H.
    Am J Med Genet; 1990 Feb; 35(2):269-73. PubMed ID: 2178418
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  • 7. Deletions of the long arm of chromosome 6: two new cases and review of the literature.
    Young RS, Fidone GS, Reider-Garcia PA, Hansen KL, McCombs JL, Moore CM.
    Am J Med Genet; 1985 Jan; 20(1):21-9. PubMed ID: 3881954
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  • 8. Partial duplication of distal 17q.
    Bridge J, Sanger W, Mosher G, Buehler B, Hearty C, Olney A, Fordyce R.
    Am J Med Genet; 1985 Oct; 22(2):229-35. PubMed ID: 4050855
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  • 9. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
    Stratton RF, Dobyns WB, Greenberg F, DeSana JB, Moore C, Fidone G, Runge GH, Feldman P, Sekhon GS, Pauli RM.
    Am J Med Genet; 1986 Jul; 24(3):421-32. PubMed ID: 3728561
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  • 10. Deletion of the distal long arm of chromosome 1: a definable syndrome.
    Johnson VP, Heck LJ, Carter GA, Flom JO.
    Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
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  • 12. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.
    Wieczorek D, Krause M, Majewski F, Albrecht B, Horn D, Riess O, Gillessen-Kaesbach G.
    Eur J Hum Genet; 2000 Jul; 8(7):519-26. PubMed ID: 10909852
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  • 13. 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 Jul; 24(3):158-61. PubMed ID: 6974525
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  • 15. 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
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  • 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
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  • 17. Partial deletion of chromosome 6p: delineation of the syndrome.
    Palmer CG, Bader P, Slovak ML, Comings DE, Pettenati MJ.
    Am J Med Genet; 1991 May 01; 39(2):155-60. PubMed ID: 2063917
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  • 18. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32).
    Martin-Pont B, Pilczer C, Dandine M, Tamboise A.
    Ann Genet; 1985 May 01; 28(4):251-3. PubMed ID: 3879441
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  • 19. 7q deletion syndrome (7q32 leads to 7qter).
    Harris EL, Wappner RS, Palmer CG, Hall B, Dinno N, Seashore MR, Breg WR.
    Clin Genet; 1977 Oct 01; 12(4):233-8. PubMed ID: 912940
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  • 20. Interstitial deletion 2q31 leads to q33.
    Buchanan PD, Rhodes RL, Stevenson CE.
    Am J Med Genet; 1983 May 01; 15(1):121-6. PubMed ID: 6683075
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