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Journal Abstract Search

180 related items for PubMed ID: 7710255

  • 1. Terminal deletion of 6p: report of a new case.
    Plaja A, Vidal R, Soriano D, Bou X, Vendrell T, Mediano C, Pueyo JM, Labraña X, Sarret E.
    Ann Genet; 1994; 37(4):196-9. PubMed ID: 7710255
    [Abstract] [Full Text] [Related]

  • 2. Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).
    Gibbons B, Tan SY, Kee SK, Quaife R, Lim ST.
    Am J Med Genet; 1999 Sep 17; 86(3):289-93. PubMed ID: 10482883
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  • 3. 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 17; 37(4):475-7. PubMed ID: 2260591
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  • 5. Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.
    Obregon MG, Mingarelli R, Digilio MC, Zelante L, Giannotti A, Sabatino G, Dallapiccola B.
    Ann Genet; 1992 Dec 17; 35(4):208-12. PubMed ID: 1296516
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  • 6. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.
    Taysi K, Strauss AW, Yang V, Padmalatha C, Marshall RE.
    Ann Genet; 1982 Dec 17; 25(3):141-4. PubMed ID: 6982660
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  • 9. 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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  • 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 May 01; 24(3):158-61. PubMed ID: 6974525
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  • 11. Unbalanced 4;6 translocation and progressive renal disease.
    Pierpont ME, Hentges AS, Gears LJ, Hirsch B, Sinaiko A.
    Am J Med Genet; 2000 Nov 27; 95(3):275-80. PubMed ID: 11102935
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  • 12. Interstitial deletion of long arm of chromosome 13.
    Carnevale A, Frias S, Alcantar R.
    Ann Genet; 1984 Nov 27; 27(1):49-52. PubMed ID: 6609673
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  • 13. Trisomy 22: no longer an enigma.
    Kukolich MK, Kulharya A, Jalal SM, Drummond-Borg M.
    Am J Med Genet; 1989 Dec 27; 34(4):541-4. PubMed ID: 2624265
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  • 14. Short clinical report: a new case with de novo partial 9p monosomy.
    Nagy E, Bod M, Nemeth I, Timar L.
    Acta Paediatr Hung; 1991 Dec 27; 31(4):407-13. PubMed ID: 1790023
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  • 15. The syndrome of ring chromosome 12.
    Scribanu N, McCullars EB, Baumiller RC, Colon AR.
    Am J Med Genet; 1980 Dec 27; 5(2):165-70. PubMed ID: 7395909
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  • 16. Complex translocation among chromosomes 2, 3, 9, 15, 18, 20 in a patient with 3p-syndrome.
    Omrani MD, Saleh Gargari S, Azizi F, Safavi Naini N, Omrani S.
    Arch Iran Med; 2014 Jul 27; 17(7):521-2. PubMed ID: 24979567
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  • 18. 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 27; 22(4):685-94. PubMed ID: 4073121
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