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PUBMED FOR HANDHELDS

Journal Abstract Search


161 related items for PubMed ID: 728583

  • 1. Duplication (partial trisomy) of the distal long arm of chromosome 17: a new clinically recognizable chromosome disorder.
    Berberich MS, Carey JC, Lawce HJ, Hall BD.
    Birth Defects Orig Artic Ser; 1978; 14(6C):287-95. PubMed ID: 728583
    [No Abstract] [Full Text] [Related]

  • 2. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
    Cohen MM, Ornoy A, Rosenmann A, Kohn G.
    Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
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  • 3. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
    Pai GS, Thomas GH, Leonard CO, Ward JC, Valle DL, Pyeritz RE.
    Johns Hopkins Med J; 1979 Oct; 145(4):162-9. PubMed ID: 491337
    [No Abstract] [Full Text] [Related]

  • 4. Duplication 6q syndrome.
    Tipton RE, Berns JS, Johnson WE, Wilroy RS, Summitt RL.
    Am J Med Genet; 1979 Oct; 3(4):325-30. PubMed ID: 474632
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  • 5. [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].
    Turleau C, Grouchy J, Bocquentin F, Roubin M, Colin FC.
    Ann Genet; 1975 Mar; 18(1):41-4. PubMed ID: 1080037
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  • 6. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA, Mikel'saar AV, Mikel'saar RV.
    Sov Genet; 1974 Jun 01; 8(5):651-7. PubMed ID: 4413436
    [No Abstract] [Full Text] [Related]

  • 7. Malformation syndrome of duplication 12q24.1 leads to qter.
    Melnyk AR, Weiss L, Van Dyke DL, Jarvi P.
    Am J Med Genet; 1981 Jun 01; 10(4):357-65. PubMed ID: 7332029
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  • 8. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
    Ausems MG, Van Spijker HG, Dijkhuis HJ, Swanenburg De Veye HF, Bijlsma JB.
    Genet Couns; 1996 Jun 01; 7(1):61-5. PubMed ID: 8652090
    [Abstract] [Full Text] [Related]

  • 9. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
    Frankova YE, Holenova H, Braulke I.
    Monatsschr Kinderheilkd; 1991 Dec 01; 139(12):841-3. PubMed ID: 1770961
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  • 13. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
    Raoul O, Rethoré MO, Dutriliaux B, Michon L, Lejeune J.
    Ann Genet; 1975 Mar 01; 18(1):35-9. PubMed ID: 1080036
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  • 14. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
    Howard-Peebles PN, Yarbrough KM, Stoddard GR, Rary JM.
    Clin Genet; 1977 Jan 01; 11(1):46-52. PubMed ID: 830449
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  • 15. Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocation.
    Bauer K, Howard-Peebles PN, Keele D, Friedman JM.
    Am J Med Genet; 1985 Jun 01; 21(2):351-6. PubMed ID: 4014316
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  • 18. Partial trisomy of chromosome 14: (+14q-).
    Yeatman GW, Riccardi VM.
    Birth Defects Orig Artic Ser; 1976 Jun 01; 12(5):119-24. PubMed ID: 953211
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  • 19. Partial trisomy 10q occurring in a family with a reciprocal translocation t(10;18)(q25;q23).
    Kroyer S, Niebuhr E.
    Ann Genet; 1975 Mar 01; 18(1):50-5. PubMed ID: 50043
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