Complex chromosomal rearrangement involving chromosomes 11, 13 and 21
Kleczkowska, A.; Fryns, J.P.; Jaeken, J.; Van den Berghe, H.
Annales de Genetique 31(2): 126-128
1988
ISSN/ISBN: 0003-3995 PMID: 3261149 Document Number: 323072
In the present report we describe a complex chromosomal rearrangement, resulting in a distal 11p monosomy, in a 7-month-old severely retarded girl with a non-specific phenotype. In this complex chromosomal rearrangement chromosomes 11, 13 and 21 are involved in the translocation of the long arm of chromosome 21 on the short arm of chromosome 13 and translocation of the short arm and satellites of chromosome 21 on the short arm of chromosome 11.
Document emailed within 1 workday
Related Documents
Cohen, M.M. 1971: The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography Annales de Genetique 14(2): 87-96Curotti, G.; Benkhalifa, M.; Raybaud, C.; Picard, F.; Bellec, V.; Qumsiyeh, M.B. 1999: De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH Genetic Counseling 10(3): 259-264
Tanaka, N.; Ikeuchi, T.; Yara, I.; Kitahara, K. 1977: Trisomy 9p due to a maternal complex translocation involving chromosomes 4, 6 and 9 Jinrui Idengaku Zasshi. Japanese Journal of Human Genetics 21(4): 261-268
Patel, R.K.; Trivedi, A.H.; Roy, S.K.; Bhachech, S.H.; Bakshi, S.R.; Bhatavdekar, J.M.; Desai, C.J.; Patel, K.M.; Shah, P.M. 1998: A complex translocation involving chromosomes 2, 9 and 22 in a patient with chronic myeloid leukemia Journal of Experimental and Clinical Cancer Research: Cr 17(4): 443-444
Mitelman, F.; Prigogina, E.L.; Fleischman, E.W.; Frenkel, M.A.; Garwicz, S.; Heim, S.; Ilyinskaya, G.W.; Kristoffersson, U.; Mandahl, N.; Volkova, M.A. 1988: A new specific chromosomal rearrangement, t(11;20)(p15;q11), in myeloblastic leukemia with maturation Leukemia 2(7): 430-432
Szemere, G. 1982: Cytological evidence of chromosomal rearrangement in the second meiotic division after exposure to X-rays Acta Biologica Academiae Scientiarum Hungaricae 33(1): 61-67
Caligiuri, M.A.; Schichman, S.A.; Strout, M.P.; Mrózek, K.; Baer, M.R.; Frankel, S.R.; Barcos, M.; Herzig, G.P.; Croce, C.M.; Bloomfield, C.D. 1994: Molecular rearrangement of the ALL-1 gene in acute myeloid leukemia without cytogenetic evidence of 11q23 chromosomal translocations Cancer Research 54(2): 370-373
Van Krieken, J.H.; McKeithan, T.W.; Raghoebier, S.; Medeiros, L.J.; Kluin, P.M.; Raffeld, M. 1990: Chromosomal translocation t(14;19) as indicated by bcl-3 rearrangement is a rare phenomenon in non-Hodgkin's lymphoma and chronic lymphocytic leukemia: a molecular genetic analysis of 176 cases Leukemia 4(12): 811-812
Hori, T. 1986: Fragile sites on human chromosomes and cancer-specific chromosomal rearrangements Gan to Kagaku Ryoho. Cancer and ChemoTherapy 13(3 Part 2): 667-676
Li, S.Y.; Jong, R.H.; Chow, M.C.; Jou, T.C. 1984: Double balanced de novo translocations involving chromosomes 4/15 and 5/12 in a mentally retarded boy Proceedings of the National Science Council Republic of China. Part B Life Sciences 8(1): 54-59
Heim, S. 1991: Epidemiological clues to leukaemias involving specific chromosomal abnormalities Leukemia 5(9): 823-824
Melo, D.G.; Huber, J.; Giuliani, L.R.; Mazzucatto, L.F.; Riegel, M.; Pina-Neto, J.M. 2004: De novo complex chromosome rearrangement: a study of two patients Genetic Counseling 15(3): 303-310
De Braekeleer, M.; Morel, Fédéric.; Le Bris, M-Josée.; Herry, Aèle.; Douet-Guilbert, N. 2005: The MLL gene and translocations involving chromosomal band 11q23 in acute leukemia Anticancer Research 25(3b): 1931-1944
Kabisch, R.; Bautz, E.K. 1983: Differential distribution of RNA polymerase B and nonhistone chromosomal proteins in polytene chromosomes of Drosophila melanogaster EMBO Journal 2(3): 395-402
Taillemite, J.L.; Baheux-Morlier, G.; Cathelineau, L.; Roux, C. 1973: Crying cat disease associated with complex chromosome rearrangement in a dizygotic twin Annales de Genetique 16(2): 127-130
Ino, T.; Hirano, M. 1992: Chromosomal translocations involving immunoglobulin or T-cell receptor genes in lymphoid malignancy Nihon Rinsho. Japanese Journal of Clinical Medicine 50(6): 1327-1334
Rubtsov, N.B.; Grafodatskiĭ, A.S.; Matveeva, V.G.; Nesterova, T.B.; Kul'bakina, N.A. 1988: Genome mapping of the silver fox. I. Determination of the chromosomal location of 8 fox genes and the search for homologous regions on fox and human chromosomes Genetika 24(1): 69-79
Verma, R.S.; Dosik, H. 1981: Human chromosomal heteromorphism in American blacks. V. Racial differences in size variation of the short arm of acrocentric chromosomes Experientia 37(3): 241-243
Akervall, J.; Borg, A.; Dictor, M.; Jin, C.; Jin, Y.; Tanner, M.; Isola, J.; Mertens, F.; Wennerberg, J. 2002: Chromosomal translocations involving 11q13 contribute to cyclin D1 overexpression in squamous cell carcinoma of the head and neck International Journal of Oncology 20(1): 45-52
VanNess, B.G.; Shapiro, M.; Kelley, D.E.; Perry, R.P.; Weigert, M.; D'Eustachio, P.; Ruddle, F. 1983: Aberrant rearrangement of the kappa light-chain locus involving the heavy-chain locus and chromosome 15 in a mouse plasmacytoma Nature 301(5899): 425-427