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Journal Abstract Search

76 related items for PubMed ID: 1733172

  • 1. 11q;22q translocation: third case of imbalance not due to 3:1 nondisjunction in first meiosis.
    Lurie IW, Podleschuk LV.
    Am J Med Genet; 1992 Jan 15; 42(2):216. PubMed ID: 1733172
    [No Abstract] [Full Text] [Related]

  • 2. Second meiotic nondisjunction of the rearranged chromosome in a familial reciprocal 5/13 translocation.
    Masuno M, Cholsong Y, Kuwahara T, Shimizu N, Yamaguchi S, Kawabata I, Tamaya T, Morishita Y, Yoshimi N, Orii T.
    Am J Med Genet; 1991 Oct 01; 41(1):32-4. PubMed ID: 1951460
    [Abstract] [Full Text] [Related]

  • 3. Unbalanced karyotype due to adjacent 1 segregation of t(11;22)(q23.3;q13.2).
    Tachdjian G, Muti C, Gaudelus J, Druart L, Martin B, Tamboise E, Nessmann C.
    Ann Genet; 1992 Oct 01; 35(4):231-3. PubMed ID: 1296521
    [Abstract] [Full Text] [Related]

  • 4. The translocation 11q;22q: a novel unbalanced karyotype.
    Abeliovich D, Carmi R.
    Am J Med Genet; 1990 Oct 01; 37(2):288. PubMed ID: 2248300
    [No Abstract] [Full Text] [Related]

  • 5. [Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].
    Stankiewicz P, Korniszewski L, Bocian E, Stańczak H.
    Pediatr Pol; 1996 Mar 01; 71(3):241-5. PubMed ID: 8966096
    [Abstract] [Full Text] [Related]

  • 6. Involvement of 3:1 disjunction in the common reciprocal translocation t(11;22) (q23.3;q11.2).
    Chandley AC.
    Hum Genet; 1992 Mar 01; 90(1-2):191-2. PubMed ID: 1427783
    [No Abstract] [Full Text] [Related]

  • 7. 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 01; 88(4):482-3. PubMed ID: 1740326
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 83(3):287-8. PubMed ID: 2793173
    [Abstract] [Full Text] [Related]

  • 9. [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 01; 28(10):129-35. PubMed ID: 1468637
    [Abstract] [Full Text] [Related]

  • 10. [11q trisomy: apropos of 2 cases].
    Noir A, Leroux M, Bresson JL, Menget A, Burguet A, Raffi A.
    Pediatrie; 1987 Oct 01; 42(6):441-4. PubMed ID: 3438103
    [Abstract] [Full Text] [Related]

  • 11. Duplication of distal 22q.
    Abeliovich D, Maor E, Bashan N, Carmi R.
    Am J Med Genet; 1989 Mar 01; 32(3):346-9. PubMed ID: 2729354
    [Abstract] [Full Text] [Related]

  • 12. Diaphragmatic hernia and Fryns syndrome phenotype in partial trisomy 22.
    de Beaufort C, Schneider F, Chafai R, Colette JM, Delneste D, Pierquin G.
    Genet Couns; 2000 Mar 01; 11(2):181-2. PubMed ID: 10893671
    [No Abstract] [Full Text] [Related]

  • 13. [11q distal trisomy due to a familial 11;18 translocation].
    Menéndez I, Rivera H, Morales E, Juan J, Jiménez M.
    Bol Med Hosp Infant Mex; 1990 Nov 01; 47(11):792-4. PubMed ID: 2285470
    [Abstract] [Full Text] [Related]

  • 14. Duplication 11 (q22----qter) in an infant. A case report with review.
    Greig F, Rosenfeld W, Verma RS, Babu KA, David K.
    Ann Genet; 1985 Nov 01; 28(3):185-8. PubMed ID: 3879155
    [Abstract] [Full Text] [Related]

  • 15. Supernumerary derivative (22) syndrome resulting from a maternal balanced translocation.
    Afroze B, Ngu LH, Roziana A, Aminah M, Noor Shahizan A.
    Singapore Med J; 2008 Dec 01; 49(12):e372-4. PubMed ID: 19122939
    [Abstract] [Full Text] [Related]

  • 16. [A syndrome of mandibulofacial dysostosis associated with a chromosome anomaly].
    Chabrolle JP, Chauveau P, Le Luyer B, Delaporte B, Coudray J.
    Ann Pediatr (Paris); 1987 Oct 01; 34(8):641-3. PubMed ID: 3688772
    [No Abstract] [Full Text] [Related]

  • 17. Hungarian case with Costello syndrome and translocation t(1,22).
    Czeizel AE, Tímár L.
    Am J Med Genet; 1995 Jul 03; 57(3):501-3. PubMed ID: 7677162
    [No Abstract] [Full Text] [Related]

  • 18. Duplication 11q and deletion 5p syndromes due to a reciprocal translocation segregating in four generations.
    Mutchinick O, Ramos Z, Sánchez F, Ruz L, Lisker R, Ovseyevitz J.
    Am J Med Genet; 1988 Jan 03; 29(1):187-92. PubMed ID: 3344767
    [Abstract] [Full Text] [Related]

  • 19. [Partial trisomy 11q 46, XX, 4q+ by translocation t (4; 11) (q35; q12)].
    Le Chevalier C, Chabrolle JP, Rossier A.
    Ann Pediatr (Paris); 1978 Nov 03; 25(9):501-4, 507. PubMed ID: 16114368
    [No Abstract] [Full Text] [Related]

  • 20. Unusual segregation of constitutional 11q;22q translocation may be explained by crossover in interchange segment, followed by 3:1 segregation at meiosis I.
    Lindenbaum RH.
    Hum Genet; 1990 Jun 03; 85(1):143. PubMed ID: 2358300
    [No Abstract] [Full Text] [Related]

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