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Journal Abstract Search

583 related items for PubMed ID: 8652089

  • 1. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
    van Buggenhout G, Decock P, Fryns JP.
    Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
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  • 3. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
    Fryns JP, Kleczkowska A, Kenis H, Decock P, Van den Berghe H.
    Ann Genet; 1989; 32(3):174-6. PubMed ID: 2573314
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  • 4. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H, Vermeesch J, Fryns JP.
    Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
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  • 5. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG, Gracia R, López Pajares I, González M, Oliver A, Peralta A.
    An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
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  • 8. Familial partial trisomy of the long arm of chromosome 10 (q24-26).
    Moreno-Fuenmayor H, Zackai EH, Mellman WJ, Aronson M.
    Pediatrics; 1975 Nov; 56(5):756-61. PubMed ID: 1196732
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  • 13. A novel duplication of chromosome (13)(q14.1q21.3) in a patient with mental retardation and microcephaly.
    Verhoeven W, Ruiter M, Egger J, Tuinier S, Smeets D.
    Genet Couns; 2009 Nov; 20(1):45-51. PubMed ID: 19400541
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  • 14. 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 Nov; 40(1):55-9. PubMed ID: 9150851
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  • 17. Partial trisomy of chromosome 18 (pter leads to q11): a discussion on the identification of the critical segment.
    San Martin V, Fernandez-Novoa C, Hevia A, Novales A, Fornell J, Galera H.
    Ann Genet; 1981 Nov; 24(4):248-50. PubMed ID: 6977308
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