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Journal Abstract Search

161 related items for PubMed ID: 6430083

  • 1. Duplication of part of chromosome 1q: clinical report and review of literature.
    Michels VV, Berseth CL, O'Brien JF, Dewald G.
    Am J Med Genet; 1984 May; 18(1):125-34. PubMed ID: 6430083
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  • 2. Dup(1q)(q42-->qter) syndrome: case report and review of literature.
    Kennerknecht I, Barbi G, Rodens K.
    Am J Med Genet; 1993 Dec 01; 47(8):1157-60. PubMed ID: 7507296
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  • 7. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
    Kímya Y, Yakut T, Egelí U, Ozerkan K.
    Prenat Diagn; 2002 Nov 01; 22(11):957-61. PubMed ID: 12424755
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  • 8. A patient with partial duplication 2q and partial deficiency 11q.
    Ho CK, Henderson KC, Bowyer FP, Eilers KB, Andrews LG.
    Am J Med Genet; 1987 Nov 01; 28(3):575-9. PubMed ID: 3322008
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  • 9. New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3.
    Wittwer B, Kircheisen R, Leutelt J, Orth U, Gal A.
    Am J Med Genet; 1996 Jul 12; 64(1):42-9. PubMed ID: 8826447
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  • 15. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to partial 1q duplication and possible 18p deletion: a study of four individuals in two families.
    Liberfarb RM, Breg WR, Atkins L, Holmes LB.
    Am J Med Genet; 1979 Jul 12; 4(1):27-37. PubMed ID: 495650
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  • 16. Partial monosomy for a 21 chromosome. Report of a new case of r(21) and review of the literature.
    Ferrante E, Vignetti P, Antonelli M, Bruni L, Bertasi S, Chessa L.
    Helv Paediatr Acta; 1983 Mar 12; 38(1):73-80. PubMed ID: 6345474
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