132 related articles for article (PubMed ID: 18424204)
21. Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development.
Schwarzbraun T; Ullmann R; Schubert M; Ledinegg M; Ofner L; Windpassinger C; Wagner K; Kroisel PM; Petek E
Cytogenet Genome Res; 2006; 115(1):84-9. PubMed ID: 16974087
[TBL] [Abstract][Full Text] [Related]
22. Molecular genetic analysis of a de novo balanced translocation t(6;17)(p21.31;q11.2) associated with hypospadias and anorectal malformation.
Mansouri MR; Carlsson B; Davey E; Nordenskjöld A; Wester T; Annerén G; Läckgren G; Dahl N
Hum Genet; 2006 Mar; 119(1-2):162-8. PubMed ID: 16395596
[TBL] [Abstract][Full Text] [Related]
23. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
[TBL] [Abstract][Full Text] [Related]
24. Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25).
Makita Y; Masuno M; Imaizumi K; Yamashita S; Ohba S; Ito D; Kuroki Y
Am J Med Genet; 1995 May; 57(1):19-21. PubMed ID: 7645592
[TBL] [Abstract][Full Text] [Related]
25. A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.
Vincent JB; Choufani S; Horike S; Stachowiak B; Li M; Dill FJ; Marshall C; Hrynchak M; Pewsey E; Ukadike KC; Friedman JM; Srivastava AK; Scherer SW
Psychiatr Genet; 2008 Jun; 18(3):101-9. PubMed ID: 18496206
[TBL] [Abstract][Full Text] [Related]
26. Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism.
Frühmesser A; Erdel M; Duba HC; Fauth C; Amberger A; Utermann G; Zschocke J; Kotzot D
Eur J Med Genet; 2013 Jul; 56(7):383-8. PubMed ID: 23608969
[TBL] [Abstract][Full Text] [Related]
27. Distinct distribution of the tensin family in the mouse kidney and small intestine.
Nishino T; Sasaki N; Chihara M; Nagasaki K; Torigoe D; Kon Y; Agui T
Exp Anim; 2012; 61(5):525-32. PubMed ID: 23095816
[TBL] [Abstract][Full Text] [Related]
28. Molecular cytogenetic characterization of multiple intrachromosomal rearrangements of chromosome 2q in a patient with Waardenburg's syndrome and other congenital defects.
Shim SH; Wyandt HE; McDonald-McGinn DM; Zackai EZ; Milunsky A
Clin Genet; 2004 Jul; 66(1):46-52. PubMed ID: 15200507
[TBL] [Abstract][Full Text] [Related]
29. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.
Guilherme RS; Cernach MC; Sfakianakis TE; Takeno SS; Nardozza LM; Rossi C; Bhatt SS; Liehr T; Melaragno MI
Cytogenet Genome Res; 2013; 141(4):317-23. PubMed ID: 23817307
[TBL] [Abstract][Full Text] [Related]
30. De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH.
Curotti G; Benkhalifa M; Raybaud C; Picard F; Bellec V; Qumsiyeh MB
Genet Couns; 1999; 10(3):259-64. PubMed ID: 10546097
[TBL] [Abstract][Full Text] [Related]
31. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH).
Hoffman DJ; Punnett HH; Pyeritz RE
Am J Perinatol; 2004 Feb; 21(2):69-71. PubMed ID: 15017469
[TBL] [Abstract][Full Text] [Related]
32. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
Laureys GG
Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
[TBL] [Abstract][Full Text] [Related]
33. De novo complex chromosome rearrangement: a study of two patients.
Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM
Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822
[TBL] [Abstract][Full Text] [Related]
34. Trisomy 7p resulting from isochromosome formation and whole-arm translocation.
Lurie IW; Schwartz MF; Schwartz S; Cohen MM
Am J Med Genet; 1995 Jan; 55(1):62-6. PubMed ID: 7702099
[TBL] [Abstract][Full Text] [Related]
35. Cytogenetic and molecular heterogeneity of 7q36/12p13 rearrangements in childhood AML.
Simmons HM; Oseth L; Nguyen P; O'Leary M; Conklin KF; Hirsch B
Leukemia; 2002 Dec; 16(12):2408-16. PubMed ID: 12454746
[TBL] [Abstract][Full Text] [Related]
36. Characterization of two ectrodactyly-associated translocation breakpoints separated by 2.5 Mb on chromosome 2q14.1-q14.2.
David D; Marques B; Ferreira C; Vieira P; Corona-Rivera A; Ferreira JC; van Bokhoven H
Eur J Hum Genet; 2009 Aug; 17(8):1024-33. PubMed ID: 19223936
[TBL] [Abstract][Full Text] [Related]
37. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
Giardino D; Corti C; Ballarati L; Finelli P; Valtorta C; Botta G; Giudici M; Grosso E; Larizza L
Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274
[TBL] [Abstract][Full Text] [Related]
38. A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.
Cetin Z; Yakut S; Clark OA; Mihci E; Berker S; Luleci G
Gene; 2013 Mar; 516(1):176-80. PubMed ID: 23262338
[TBL] [Abstract][Full Text] [Related]
39. A balanced translocation t(6;14)(q25.3;q13.2) leading to reciprocal fusion transcripts in a patient with intellectual disability and agenesis of corpus callosum.
Backx L; Seuntjens E; Devriendt K; Vermeesch J; Van Esch H
Cytogenet Genome Res; 2011; 132(3):135-43. PubMed ID: 21042007
[TBL] [Abstract][Full Text] [Related]
40. [Analysis of synaptonemal complex from a carrier with 46,XY,t(11;18) balanced translocation].
Liu JY; Wang XR; Zeng XL; Zhang CS; Song YC
Yi Chuan Xue Bao; 2004 Feb; 31(2):125-31. PubMed ID: 15473301
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
