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Journal Abstract Search

252 related items for PubMed ID: 2290435

  • 1. [Translocation trisomy 4q in 2 siblings as a sequela of paternal balanced reciprocal translocation: t(1;4)(q44;q31)].
    Bode H, Bühler EM, Wyler F, Hadzilselimovic F.
    Monatsschr Kinderheilkd; 1990 Nov; 138(11):763-6. PubMed ID: 2290435
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  • 2. Translocation/duplication of 9p onto a duplicated 4q.
    Rivera H, Figuera LE, Vasquez AI.
    Genet Couns; 1992 Nov; 3(4):201-3. PubMed ID: 1472355
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  • 3. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
    Hegmann KM, Spikes AS, Orr-Urtreger A, Shaffer LG.
    Am J Med Genet; 1996 Jan 02; 61(1):10-5. PubMed ID: 8741910
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  • 4. 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 02; 49(11):e336-9. PubMed ID: 19037546
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  • 5. [Case of partial trisomy 4p+ in a child as a result of a balanced translocation in the father].
    Patiutko RS, Kulieva LM, Egolina NA.
    Genetika; 1978 Sep 02; 14(9):1653-7. PubMed ID: 720831
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  • 6. Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
    Delaroche I, Bruni L, Giannotti A, Giampaolo R, Aebischer ML.
    Helv Paediatr Acta; 1984 May 02; 39(2):161-6. PubMed ID: 6543839
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  • 7. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M, Hemly NA, Zaki MS.
    Genet Couns; 2007 May 02; 18(2):217-26. PubMed ID: 17710874
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  • 11. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
    Francisco-Bagnariolli AM, Payão SL, Kawasaki-Oyama RS, Sabbag Filho D, Segato R, de Labio RW, Chauffaille ML, Priest JH.
    Am J Med Genet; 2001 Nov 01; 103(4):302-7. PubMed ID: 11746010
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  • 13. [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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  • 15. A translocation between chromosome 1 and 10 in a boy with mental retardation and dysmorphic features.
    Gambhir PS, Gole LA, Tembe MV, Saraph AA, Phadke MA, Khedkar VA.
    Indian Pediatr; 1991 Mar 01; 28(3):289-91. PubMed ID: 1937707
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  • 16. De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.
    Chitayat D, Fagerstrom CL, Kalousek DK, Rootman J, Taylor GP, Hall JG.
    Am J Med Genet; 1989 Jan 01; 32(1):36-41. PubMed ID: 2495721
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  • 18. The fetal phenotype of partial trisomy of the long arm of chromosome 4 (4q22----4qter).
    Petit P, Moerman P, Fryns JP.
    Genet Couns; 1991 Jan 01; 2(3):163-5. PubMed ID: 1801853
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  • 19. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
    Mégarbané A, Souraty N, Theophile D, Vekemans M, Samaras L, Ghorayeb Z.
    Ann Genet; 1997 Jan 01; 40(1):55-9. PubMed ID: 9150851
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  • 20. Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism.
    Fryns JP, Kleczkowska A, Van Den Berghe H.
    Genet Couns; 1990 Jan 01; 1(2):173-7. PubMed ID: 2081001
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