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Journal Abstract Search

112 related items for PubMed ID: 3744366

  • 1. Excess of mental retardation and/or congenital malformation in reciprocal translocations in man.
    Steinbach P.
    Hum Genet; 1986 Aug; 73(4):379. PubMed ID: 3744366
    [No Abstract] [Full Text] [Related]

  • 2. Excess of mental retardation and/or congenital malformation in reciprocal translocations in man.
    Fryns JP, Kleczkowska A, Kubień E, Van den Berghe H.
    Hum Genet; 1986 Jan; 72(1):1-8. PubMed ID: 3943858
    [Abstract] [Full Text] [Related]

  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. [Balanced chromosome abnormalities with abnormal phenotype].
    Fryns JP.
    J Genet Hum; 1988 Jan; 36(1-2):33-6. PubMed ID: 3379377
    [Abstract] [Full Text] [Related]

  • 5. Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23).
    Dufke A, Mayrhofer H, Enders H, Kaiser P, Leipoldt M.
    Cytogenet Cell Genet; 2001 Jan; 93(3-4):168-70. PubMed ID: 11528107
    [Abstract] [Full Text] [Related]

  • 6. Twins with mental retardation and physical abnormalities: preliminary report.
    Jancar J.
    Acta Genet Med Gemellol (Roma); 1970 Jan; 19(1):311-4. PubMed ID: 5502043
    [No Abstract] [Full Text] [Related]

  • 7. Genetic syndromes among individuals with mental retardation.
    Stevenson RE, Procopio-Allen AM, Schroer RJ, Collins JS.
    Am J Med Genet A; 2003 Nov 15; 123A(1):29-32. PubMed ID: 14556243
    [Abstract] [Full Text] [Related]

  • 8. Two reciprocal translocations associated with microcephaly and retardation.
    Bell EF, Warburton D.
    J Med Genet; 1977 Apr 15; 14(2):141-2. PubMed ID: 853319
    [Abstract] [Full Text] [Related]

  • 9. On the excess of mental retardation and/or congenital malformations in apparently balanced reciprocal translocations. A critical review of the Leuven data 1966-1991.
    Fryns JP, Kleczkowska A, Kubień E, Van Den Berghe H.
    Genet Couns; 1991 Apr 15; 2(4):185-94. PubMed ID: 1799415
    [Abstract] [Full Text] [Related]

  • 10. Chromosomal aberrations, subtelomeric defects, and mental retardation.
    Baralle D.
    Lancet; 2001 Jul 07; 358(9275):7-8. PubMed ID: 11454368
    [No Abstract] [Full Text] [Related]

  • 11. Double balanced de novo translocations involving chromosomes 4/15 and 5/12 in a mentally retarded boy.
    Li SY, Jong RH, Chow MC, Jou TC.
    Proc Natl Sci Counc Repub China B; 1984 Jan 07; 8(1):54-9. PubMed ID: 6531417
    [Abstract] [Full Text] [Related]

  • 12. Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a approximately 0.5-Mb submicroscopic deletion in a patient with mild mental retardation.
    Borg K, Stankiewicz P, Bocian E, Kruczek A, Obersztyn E, Lupski JR, Mazurczak T.
    Hum Genet; 2005 Nov 07; 118(2):267-75. PubMed ID: 16160854
    [Abstract] [Full Text] [Related]

  • 13. Fluorescent in situ hybridization: use of whole chromosome paint probes to identify unbalanced chromosome translocations.
    Kraker WJ, Borell TJ, Schad CR, Pennington MJ, Karnes PS, Dewald GW, Jenkins RB.
    Mayo Clin Proc; 1992 Jul 07; 67(7):658-62. PubMed ID: 1434900
    [Abstract] [Full Text] [Related]

  • 14.
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    [No Abstract] [Full Text] [Related]

  • 15. Two Robertsonian translocations in a boy with mental retardation.
    Lieber E, Shah P.
    J Med Genet; 1982 Jun 07; 19(3):229-32. PubMed ID: 7108921
    [Abstract] [Full Text] [Related]

  • 16. Mixoploidy combined with aneuploidy in a 13 year-old patient with severe multiple congenital abnormalities and intellectual disability.
    van Zutven LJCM, Mancini GMS, Bindels-de Heus KGCB, van den Akker ELT, Hulsman LOM, Smit M, Berna Beverloo H.
    Am J Med Genet A; 2018 Feb 07; 176(2):492-495. PubMed ID: 29226581
    [No Abstract] [Full Text] [Related]

  • 17. A case of partial trisomy 17 resulting from X-autosomal translocation.
    Yamamoto Y, Endo Y, Kuroki Y.
    J Med Genet; 1979 Oct 07; 16(5):395-9. PubMed ID: 513087
    [Abstract] [Full Text] [Related]

  • 18. XLMR genes: update 1990.
    Neri G, Gurrieri F, Gal A, Lubs HA.
    Am J Med Genet; 1991 Oct 07; 38(2-3):186-9. PubMed ID: 2018056
    [Abstract] [Full Text] [Related]

  • 19. 13q33.2 deletion: a rare cause of ambiguous genitalia in a male newborn with growth restriction.
    Andresen JH, Aftimos S, Doherty E, Love DR, Battin M.
    Acta Paediatr; 2010 May 07; 99(5):784-786. PubMed ID: 20105145
    [Abstract] [Full Text] [Related]

  • 20. De novo simultaneous reciprocal translocation and deletion.
    Fries K, Mundel G, Rosenblatt M.
    J Med Genet; 1978 Apr 07; 15(2):152-4. PubMed ID: 641951
    [Abstract] [Full Text] [Related]

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