167 related articles for article (PubMed ID: 20179746)
61. A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities.
Youings S; Ellis K; Ennis S; Barber J; Jacobs P
Am J Med Genet A; 2004 Apr; 126A(1):46-60. PubMed ID: 15039973
[TBL] [Abstract][Full Text] [Related]
62. Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.
Kogo H; Inagaki H; Ohye T; Kato T; Emanuel BS; Kurahashi H
Nucleic Acids Res; 2007; 35(4):1198-208. PubMed ID: 17264116
[TBL] [Abstract][Full Text] [Related]
63. Sperm analysis by FISH in a case of t(17; 22) (q11; q12) balanced translocation: case report.
Geneix A; Schubert B; Force A; Rodet K; Briançon G; Boucher D
Hum Reprod; 2002 Feb; 17(2):325-31. PubMed ID: 11821272
[TBL] [Abstract][Full Text] [Related]
64. Paternal balanced reciprocal translocation t(9;22)(q34.3;q11.2) resulting in an infant with features of the 9q subtelomere and the 22q11 deletion syndromes due to 3:1 meiotic segregation and tertiary monosomy.
McGoey RR; Lacassie Y
Am J Med Genet A; 2009 Nov; 149A(11):2538-42. PubMed ID: 19876901
[TBL] [Abstract][Full Text] [Related]
65. Restricted chromosome breakpoint sites on 11q22-q23.1 and 11q25 in various hematological malignancies without MLL/ALL-1 gene rearrangement.
Tanaka K; Eguchi M; Eguchi-Ishimae M; Hasegawa A; Ohgami A; Kikuchi M; Kyo T; Asaoku H; Dohy H; Kamada N
Cancer Genet Cytogenet; 2001 Jan; 124(1):27-35. PubMed ID: 11165319
[TBL] [Abstract][Full Text] [Related]
66. 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
[TBL] [Abstract][Full Text] [Related]
67. Cloning of ALL-1, the locus involved in leukemias with the t(4;11)(q21;q23), t(9;11)(p22;q23), and t(11;19)(q23;p13) chromosome translocations.
Cimino G; Moir DT; Canaani O; Williams K; Crist WM; Katzav S; Cannizzaro L; Lange B; Nowell PC; Croce CM
Cancer Res; 1991 Dec; 51(24):6712-4. PubMed ID: 1835902
[TBL] [Abstract][Full Text] [Related]
68. A novel 5-way translocation t(9;11;13;19;22) in a case of chronic-phase chronic myeloid leukemia.
Vaidya S; Joshi D; Ghosh K; Chakrabarti P; Vundinti BR
Hum Pathol; 2013 Oct; 44(10):2365-9. PubMed ID: 23759653
[TBL] [Abstract][Full Text] [Related]
69. Involvement of 3:1 disjunction in the common reciprocal translocation t(11;22) (q23.3;q11.2).
Chandley AC
Hum Genet; 1992; 90(1-2):191-2. PubMed ID: 1427783
[No Abstract] [Full Text] [Related]
70. Malignant hematopoietic cell lines: in vitro models for the study of MLL gene alterations.
Drexler HG; Quentmeier H; MacLeod RA
Leukemia; 2004 Feb; 18(2):227-32. PubMed ID: 14671638
[TBL] [Abstract][Full Text] [Related]
71. Sperm segregation analysis of a (13;22) Robertsonian translocation carrier by FISH: a comparison of locus-specific probe and whole chromosome painting.
Anahory T; Hamamah S; Andréo B; Hédon B; Claustres M; Sarda P; Pellestor F
Hum Reprod; 2005 Jul; 20(7):1850-4. PubMed ID: 15845597
[TBL] [Abstract][Full Text] [Related]
72. Parental origin determination in thirty de novo Robertsonian translocations.
Shaffer LG; Jackson-Cook CK; Stasiowski BA; Spence JE; Brown JA
Am J Med Genet; 1992 Aug; 43(6):957-63. PubMed ID: 1357969
[TBL] [Abstract][Full Text] [Related]
73. Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.
Funke B; Edelmann L; McCain N; Pandita RK; Ferreira J; Merscher S; Zohouri M; Cannizzaro L; Shanske A; Morrow BE
Am J Hum Genet; 1999 Mar; 64(3):747-58. PubMed ID: 10053009
[TBL] [Abstract][Full Text] [Related]
74. Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis I.
Petković I; de Capoa A; Giancotti P; Barisić I
Clin Genet; 1996 Dec; 50(6):515-9. PubMed ID: 9147886
[TBL] [Abstract][Full Text] [Related]
75. Acute leukaemia and myelodysplastic syndromes with chromosomal rearrangement involving 11q23 locus, but not
Zuo W; Wang SA; DiNardo C; Yabe M; Li S; Medeiros LJ; Tang G
J Clin Pathol; 2017 Mar; 70(3):244-249. PubMed ID: 27496968
[TBL] [Abstract][Full Text] [Related]
76. Robertsonian translocations and abnormal phenotypes. Groupe de Cytogénéticiens Français.
Ann Genet; 1989; 32(1):5-9. PubMed ID: 2665630
[TBL] [Abstract][Full Text] [Related]
77. Molecular characterization of a variant Ph1 translocation t(9;22;11) (q34;q11;q13) in chronic myelogenous leukemia (CML) reveals the translocation of the 3'-part of BCR gene to the chromosome band 11q13.
Koduru PR; Goh JC; Pergolizzi RG; Lichtman SM; Broome JD
Oncogene; 1993 Dec; 8(12):3239-47. PubMed ID: 8247527
[TBL] [Abstract][Full Text] [Related]
78. Prenatal diagnosis of partial trisomy 22 derived from a maternal t(11; 22) (q23; q11).
Sou S; Takabayashi T; Sasaki H; Sasamoto K; Shintaku Y; Li ZJ; Ozawa N; Yajima A
Tohoku J Exp Med; 1987 Dec; 153(4):389-93. PubMed ID: 3441929
[TBL] [Abstract][Full Text] [Related]
79. Comparative mapping of the constitutional and tumor-associated 11;22 translocations.
Budarf M; Sellinger B; Griffin C; Emanuel BS
Am J Hum Genet; 1989 Jul; 45(1):128-39. PubMed ID: 2741943
[TBL] [Abstract][Full Text] [Related]
80. Molecular cloning of translocation breakpoints in a case of constitutional translocation t(11;22)(q23;q11) and preparation of probes for preimplantation genetic diagnosis.
Fung J; Munné S; Garcia J; Kim UJ; Weier HU
Reprod Fertil Dev; 1999; 11(1):17-23. PubMed ID: 10680998
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]