256 related articles for article (PubMed ID: 10577913)
21. The Recurrent t(11;22)(q23;q11.2) Can Occur as a Post-Zygotic Event.
Correll-Tash S; Conlin L; Mininger BA; Lilley B; Mennuti MT; Emanuel BS
Cytogenet Genome Res; 2018; 156(4):185-190. PubMed ID: 30566958
[TBL] [Abstract][Full Text] [Related]
22. Analysis of two translocation breakpoints and identification of a negative regulatory element in patients with Rieger's syndrome.
Trembath DG; Semina EV; Jones DH; Patil SR; Qian Q; Amendt BA; Russo AF; Murray JC
Birth Defects Res A Clin Mol Teratol; 2004 Feb; 70(2):82-91. PubMed ID: 14991915
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Meiotic and pedigree segregation analyses in carriers of t(4;8)(p16;p23.1) differing in localization of breakpoint positions at 4p subband 4p16.3 and 4p16.1.
Midro AT; Zollino M; Wiland E; Panasiuk B; Iwanowski PS; Murdolo M; Śmigiel R; Sąsiadek M; Pilch J; Kurpisz M
J Assist Reprod Genet; 2016 Feb; 33(2):189-97. PubMed ID: 26637389
[TBL] [Abstract][Full Text] [Related]
25. Fine-mapping of cytogenetically undetectable EWS/ERG fusions on DNA fibers of Ewing tumors.
Hattinger CM; Rumpler S; Kovar H; Ambros PF
Cytogenet Cell Genet; 2001; 93(1-2):29-35. PubMed ID: 11474174
[TBL] [Abstract][Full Text] [Related]
26. Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype.
Vervoort VS; Viljoen D; Smart R; Suthers G; DuPont BR; Abbott A; Schwartz CE
J Med Genet; 2002 Dec; 39(12):893-9. PubMed ID: 12471201
[TBL] [Abstract][Full Text] [Related]
27. Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.
Dawson AJ; Mears AJ; Chudley AE; Bech-Hansen T; McDermid H
J Med Genet; 1996 Nov; 33(11):952-6. PubMed ID: 8950677
[TBL] [Abstract][Full Text] [Related]
28. Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.
Edelmann L; Pandita RK; Morrow BE
Am J Hum Genet; 1999 Apr; 64(4):1076-86. PubMed ID: 10090893
[TBL] [Abstract][Full Text] [Related]
29. Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation.
Willett-Brozick JE; Savul SA; Richey LE; Baysal BE
Hum Genet; 2001 Aug; 109(2):216-23. PubMed ID: 11511928
[TBL] [Abstract][Full Text] [Related]
30. A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).
Sheridan MB; Kato T; Haldeman-Englert C; Jalali GR; Milunsky JM; Zou Y; Klaes R; Gimelli G; Gimelli S; Gemmill RM; Drabkin HA; Hacker AM; Brown J; Tomkins D; Shaikh TH; Kurahashi H; Zackai EH; Emanuel BS
Am J Hum Genet; 2010 Aug; 87(2):209-18. PubMed ID: 20673865
[TBL] [Abstract][Full Text] [Related]
31. Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.
Ou Z; Stankiewicz P; Xia Z; Breman AM; Dawson B; Wiszniewska J; Szafranski P; Cooper ML; Rao M; Shao L; South ST; Coleman K; Fernhoff PM; Deray MJ; Rosengren S; Roeder ER; Enciso VB; Chinault AC; Patel A; Kang SH; Shaw CA; Lupski JR; Cheung SW
Genome Res; 2011 Jan; 21(1):33-46. PubMed ID: 21205869
[TBL] [Abstract][Full Text] [Related]
32. 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
[TBL] [Abstract][Full Text] [Related]
33. Preimplantation genetic diagnosis outcomes and meiotic segregation analysis of robertsonian translocation carriers.
Ko DS; Cho JW; Lee HS; Kim JY; Kang IS; Yang KM; Lim CK
Fertil Steril; 2013 Apr; 99(5):1369-76. PubMed ID: 23312224
[TBL] [Abstract][Full Text] [Related]
34. Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers.
Ogur G; Van Assche E; Vegetti W; Verheyen G; Tournaye H; Bonduelle M; Van Steirteghem A; Liebaers I
Mol Hum Reprod; 2006 Mar; 12(3):209-15. PubMed ID: 16524928
[TBL] [Abstract][Full Text] [Related]
35. Reciprocal chromosome translocations involving short arm of chromosome 9 as a risk factor of unfavorable pregnancy outcomes after meiotic malsegregation 2:2.
Panasiuk B; Danik J; Lurie IW; Stasiewicz-Jarocka B; Leśniewicz R; Sawicka A; Kałuzewski B; Midro AT
Adv Med Sci; 2009; 54(2):203-10. PubMed ID: 19758973
[TBL] [Abstract][Full Text] [Related]
36. Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation.
Wlodarska I; Selleri L; La Starza R; Paternotte C; Evans GA; Boogaerts M; Van den Berghe H; Mecucci C
Genes Chromosomes Cancer; 1999 Mar; 24(3):199-206. PubMed ID: 10451699
[TBL] [Abstract][Full Text] [Related]
37. [Meiotic segregation results of male reciprocal chromosome translocations].
Huang XF; Xiao SQ; Fei QJ; Zhang W; Zhang LY; Yang X; Ye BL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Apr; 24(2):217-20. PubMed ID: 17407087
[TBL] [Abstract][Full Text] [Related]
38. MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site.
Slater DJ; Hilgenfeld E; Rappaport EF; Shah N; Meek RG; Williams WR; Lovett BD; Osheroff N; Autar RS; Ried T; Felix CA
Oncogene; 2002 Jul; 21(30):4706-14. PubMed ID: 12096348
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia.
Super HG; Strissel PL; Sobulo OM; Burian D; Reshmi SC; Roe B; Zeleznik-Le NJ; Diaz MO; Rowley JD
Genes Chromosomes Cancer; 1997 Oct; 20(2):185-95. PubMed ID: 9331569
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
