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Journal Abstract Search

78 related items for PubMed ID: 2742241

  • 1. [8:11 translocation. A familial study].
    Vargas de los Monteros MT, Fernández-Novoa García MC, González González MV, San Martín Díez MV, Fernández Ortega JM.
    An Esp Pediatr; 1989 Apr; 30(4):303-5. PubMed ID: 2742241
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  • 2. [An excess of mental retardation and/or congenital malformations in carriers of reciprocal translocations. A difficult and delicate problem in genetic counseling].
    Fryns JP, Kleczkowska A, Van den Berghe H.
    J Genet Hum; 1987 Jan; 35(1):47-50. PubMed ID: 3559523
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  • 3. [Familial balanced chromosome translocation t(12;13) in a family with several deformed stillbirths].
    Bommer C, Körner H.
    Zentralbl Gynakol; 1982 Jan; 104(24):1578-83. PubMed ID: 6892078
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  • 4. 8q22-->qter duplication in a child with multiple congenital malformations: case report.
    Sasiadek M, Stembalska A, Schlade K, Zych M.
    Med Sci Monit; 2000 Jan; 6(1):141-4. PubMed ID: 11208302
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  • 5. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.
    Bacino CA, Kashork CD, Davino NA, Shaffer LG.
    Am J Med Genet; 2000 Jun 05; 92(4):250-5. PubMed ID: 10842290
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  • 6. Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.
    Wheeler PG, Weaver DD, Palmer CG.
    Am J Med Genet; 1995 Feb 13; 55(4):462-5. PubMed ID: 7762587
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  • 13. Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis.
    Prontera P, Buldrini B, Aiello V, Gruppioni R, Bonfatti A, Venti G, Ferlini A, Sensi A, Calzolari E, Donti E.
    Prenat Diagn; 2006 Jun 13; 26(6):571-6. PubMed ID: 16683276
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  • 18. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG, Spikes AS, Macha M, Dunn R.
    J Reprod Med; 1996 May 13; 41(5):367-71. PubMed ID: 8725766
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  • 19. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.
    Pazarbaşi A, Demirhan O, Turgut M, Güzel I, Taştemir D.
    Genet Couns; 2008 May 13; 19(3):301-8. PubMed ID: 18990986
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