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Journal Abstract Search

188 related items for PubMed ID: 3943858

  • 21. Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype.
    Sismani C, Kitsiou-Tzeli S, Ioannides M, Christodoulou C, Anastasiadou V, Stylianidou G, Papadopoulou E, Kanavakis E, Kosmaidou-Aravidou Z, Patsalis PC.
    Mol Cytogenet; 2008 Jul 21; 1():15. PubMed ID: 18644119
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  • 24. Autosomal reciprocal translocations and 13/14 translocations: a population study.
    Nielsen J, Rasmussen K.
    Clin Genet; 1976 Sep 21; 10(3):161-77. PubMed ID: 786515
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  • 26. Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and delection 10q.
    Larson LM, Wasdahl WA, Saumur JH, Coleman ML, Hall JG, Dolan CR, Schutta CJ.
    Clin Genet; 1982 Mar 21; 21(3):187-95. PubMed ID: 7094394
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  • 27. The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families.
    Iselius L, Lindsten J, Aurias A, Fraccaro M, Bastard C, Bottelli AM, Bui TH, Caufin D, Dalprà L, Delendi N.
    Hum Genet; 1983 Mar 21; 64(4):343-55. PubMed ID: 6618487
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  • 29. Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.
    Zackai EH, Emanuel BS.
    Am J Med Genet; 1980 Mar 21; 7(4):507-21. PubMed ID: 7211960
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  • 30. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
    Balci S, Aypar E, Beksaç MS, Bartsch O.
    Genet Couns; 2009 Mar 21; 20(2):125-32. PubMed ID: 19650409
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  • 31. De novo 3q/7q translocation and associated interstitial 7q35 deletion.
    Fryns JP, Kleczkowska A, van den Berghe H.
    Clin Genet; 1988 Jan 21; 33(1):60-2. PubMed ID: 3342549
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  • 32. A case of 46,XY,t(1;13) (q24;q32) with mental retardation.
    Wilbur L, Curcuru-Giordano FM, Krishna SG, Kardon NB, Jenkins EC.
    Hum Genet; 1977 Jun 30; 37(2):239-42. PubMed ID: 885541
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  • 33. [Chromosome translocations: study of 232 cases originating from 144 families].
    Gillerot Y, Koulischer L, Jauniaux E.
    J Genet Hum; 1988 Jan 30; 36(1-2):45-57. PubMed ID: 2967887
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  • 34. Cytogenetic survey in couples with recurrent fetal wastage.
    Fryns JP, Kleczkowska A, Kubień E, Petit P, Van den Berghe H.
    Hum Genet; 1984 Jan 30; 65(4):336-54. PubMed ID: 6693122
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  • 35. Aniridia, mental retardation and an unbalanced reciprocal translocation of chromosomes 8 and 11 with an interstitial deletion of 11p.
    Gödde-Salz E, Behnke H.
    Eur J Pediatr; 1981 Mar 30; 136(1):93-6. PubMed ID: 7215394
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  • 36. Segregation analysis in reciprocal translocation carriers.
    Petrosky DL, Borgaonkar DS.
    Am J Med Genet; 1984 Sep 30; 19(1):137-59. PubMed ID: 6496566
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  • 37. Parental origin of de novo cytogenetically balanced reciprocal non-Robertsonian translocations.
    Höckner M, Spreiz A, Frühmesser A, Tzschach A, Dufke A, Rittinger O, Kalscheuer V, Singer S, Erdel M, Fauth C, Grossmann V, Utermann G, Zschocke J, Kotzot D.
    Cytogenet Genome Res; 2012 Sep 30; 136(4):242-5. PubMed ID: 22516930
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  • 38. Family with three apparently balanced t(3;15) (p27;q22) translocation carriers. Association with deficits in language acquisition and mental retardation: a possible example of position effect in man.
    Gardner LI, Neu RL, Shah RS, Pinto W, Co M, Lehr ER, Barg GA.
    Am J Dis Child; 1979 Oct 30; 133(10):1002-5. PubMed ID: 495587
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  • 39. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.
    Daniel A, Hook EB, Wulf G.
    Am J Med Genet; 1989 May 30; 33(1):14-53. PubMed ID: 2750783
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  • 40. Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23).
    Tranebjaerg L, Baekmark UB, Dyhr-Nielsen M, Kreiborg S.
    Clin Genet; 1987 Aug 30; 32(2):137-43. PubMed ID: 3652493
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