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Journal Abstract Search

93 related items for PubMed ID: 6977302

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  • 27. Presence of Y chromosome sequences and their effect on the phenotype of six patients with Y chromosome anomalies.
    Shankman S, Spurdle AB, Morris D, Rosendorff J, Marques I, Bernstein R, Ramsay M.
    Am J Med Genet; 1995 Jan 30; 55(3):269-75. PubMed ID: 7726221
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  • 30. [New chromosomal syndromes].
    Duca D, Meilă P, Ursuleanu I, Maximillian C.
    Rev Pediatr Obstet Ginecol Pediatr; 1978 Jan 30; 27(4):343-62. PubMed ID: 107564
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  • 31. The usefulness of NOR and RFA banding in prenatal diagnosis: a case report.
    Sciorra LJ, Rajendra B, Cummings E, Ekblom L, Lee M.
    Am J Med Genet; 1981 Jan 30; 10(2):147-9. PubMed ID: 7315871
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  • 32. [Mosaic variant of the translocation form of syndrome 18q-].
    Badalian LO, Dement'eva GM, Malygina NA, Mutovin GR, Petrukhin AS.
    Genetika; 1981 Jan 30; 17(10):1867-71. PubMed ID: 7198075
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  • 33. [Further study on the nature of a multicentury small Y chromosome (author's transl)].
    Genest P.
    Ann Genet; 1981 Jan 30; 24(3):165-6. PubMed ID: 6974527
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  • 34. Need for search for cryptic translocation in parents with several children affected with MCA: report of a cryptic translocation (10;14) detected by FISH.
    Delneste D, Vamos E, Pierquin G, Hayez-Delatte F, Van Regemorter N.
    Genet Couns; 1998 Jan 30; 9(2):97-102. PubMed ID: 9664205
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  • 36. Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features.
    Kleefstra T, van de Zande G, Merkx G, Mieloo H, Hoovers JM, Smeets D.
    Eur J Hum Genet; 2000 Aug 30; 8(8):637-40. PubMed ID: 10951526
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  • 37. [Discovery of analogous balanced translocation syndrome and its clinical genetics research].
    Cheng SX, Liu L, Wu HW.
    Hunan Yi Ke Da Xue Xue Bao; 2003 Apr 30; 28(2):95-8. PubMed ID: 12934345
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  • 39. [Y chromosome rearrangement and phenotypical consequences].
    Mujica P, Abbadi N, Formiga LD, Gilgenkrantz S.
    J Genet Hum; 1988 Jan 30; 36(1-2):69-73. PubMed ID: 3379381
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  • 40. [Terminal 1q deletion by translocation t(1;20)pat, confirmed by in situ hybridization].
    López-Ginés C, Gil-Benso R, Gregori-Romero MA, Paredes-Cencillo C, Castelló-Pomares M, Llombart-Bosch A.
    An Esp Pediatr; 1998 Mar 30; 48(3):309-11. PubMed ID: 9608096
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