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Journal Abstract Search

91 related items for PubMed ID: 2358300

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  • 2. Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.
    Lockwood DH, Farrier A, Hecht F, Allanson J.
    Hum Genet; 1989 Oct; 83(3):287-8. PubMed ID: 2793173
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  • 5. Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.
    Lindblom A, Sandelin K, Iselius L, Dumanski J, White I, Nordenskjöld M, Larsson C.
    Am J Hum Genet; 1994 May; 54(5):871-6. PubMed ID: 8178827
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  • 6. The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte.
    Simi P, Ceccarelli M, Barachini A, Floridia G, Zuffardi O.
    Hum Genet; 1992 Feb; 88(4):482-3. PubMed ID: 1740326
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  • 10. [11q trisomy: apropos of 2 cases].
    Noir A, Leroux M, Bresson JL, Menget A, Burguet A, Raffi A.
    Pediatrie; 1987 Feb; 42(6):441-4. PubMed ID: 3438103
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  • 11. High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions.
    Baumer A, Dutly F, Balmer D, Riegel M, Tükel T, Krajewska-Walasek M, Schinzel AA.
    Hum Mol Genet; 1998 May; 7(5):887-94. PubMed ID: 9536094
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  • 14. [Translocation 11q;22q: a clinico-cytogenetic study].
    Lur'e IV, Rumiantseva NV, Podleshchuk LV, Kozlova SI, Kulak VD, Naumchik IV, Gorelik LB, Zolotukhina TV, Kuznetsov MI.
    Genetika; 1992 Oct; 28(10):129-35. PubMed ID: 1468637
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  • 16. Crossover promotion and prevention.
    Lorenz A, Whitby MC.
    Biochem Soc Trans; 2006 Aug; 34(Pt 4):537-41. PubMed ID: 16856854
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  • 17. Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3) by triple FISH.
    Martini E, von Bergh AR, Coonen E, de Die-Smulders CE, Hopman AH, Ramaekers FC, Geraedts JP.
    Hum Genet; 1998 Feb; 102(2):157-65. PubMed ID: 9521583
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  • 18. Involvement of 3:1 disjunction in the common reciprocal translocation t(11;22) (q23.3;q11.2).
    Chandley AC.
    Hum Genet; 1992 Feb; 90(1-2):191-2. PubMed ID: 1427783
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  • 19. Sperm fluorescence in situ hybridization study of meiotic segregation and an interchromosomal effect in carriers of t(11;18).
    Vozdova M, Oracova E, Horinova V, Rubes J.
    Hum Reprod; 2008 Mar; 23(3):581-8. PubMed ID: 18182397
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  • 20. A rare case of aniridia and balanced translocation (5;11) (p15.3;q22) arising in the same subject: a challenge for genetic counseling.
    Vulcani-Freitas TM, Maciel-Guerra AT.
    Genet Couns; 2006 Mar; 17(1):49-55. PubMed ID: 16719277
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