829 related articles for article (PubMed ID: 16497571)
1. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
[TBL] [Abstract][Full Text] [Related]
2. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P
Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206
[TBL] [Abstract][Full Text] [Related]
3. Familial complex chromosomal rearrangement resulting in a recombinant chromosome.
Berend SA; Bodamer OA; Shapira SK; Shaffer LG; Bacino CA
Am J Med Genet; 2002 May; 109(4):311-7. PubMed ID: 11992486
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
Batista DA; Pai GS; Stetten G
Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 8q22-->qter duplication in a child with multiple congenital malformations: case report.
Sasiadek M; Stembalska A; Schlade K; Zych M
Med Sci Monit; 2000; 6(1):141-4. PubMed ID: 11208302
[TBL] [Abstract][Full Text] [Related]
8. DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.
Demczuk S; Aurias A
Ann Genet; 1995; 38(2):59-76. PubMed ID: 7486827
[TBL] [Abstract][Full Text] [Related]
9. Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.
Röthlisberger B; Kotzot D; Brecevic L; Koehler M; Balmer D; Binkert F; Schinzel A
Eur J Hum Genet; 1999 Dec; 7(8):873-83. PubMed ID: 10602362
[TBL] [Abstract][Full Text] [Related]
10. Complex chromosome rearrangements and congenital anomalies.
Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH.
Roos A; Rudnik-Schöneborn S; Eggermann K; Eggermann T; Senderek J; Schwanitz G; Zerres K; Schüler HM
Eur J Med Genet; 2006; 49(6):505-10. PubMed ID: 16905374
[TBL] [Abstract][Full Text] [Related]
13. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
[TBL] [Abstract][Full Text] [Related]
15. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.
Peschka B; Leygraaf J; Hansmann D; Hansmann M; Schröck E; Ried T; Engels H; Schwanitz G; Schubert R
Prenat Diagn; 1999 Dec; 19(12):1143-9. PubMed ID: 10590433
[TBL] [Abstract][Full Text] [Related]
16. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
Shaffer LG; Spikes AS; Macha M; Dunn R
J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
[TBL] [Abstract][Full Text] [Related]
17. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
Schluth-Bolard C; Delobel B; Sanlaville D; Boute O; Cuisset JM; Sukno S; Labalme A; Duban-Bedu B; Plessis G; Jaillard S; Dubourg C; Henry C; Lucas J; Odent S; Pasquier L; Copin H; Latour P; Cordier MP; Nadeau G; Till M; Edery P; Andrieux J
Eur J Med Genet; 2009; 52(5):291-6. PubMed ID: 19505601
[TBL] [Abstract][Full Text] [Related]
18. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16.
Phelan MC; Blackburn W; Rogers RC; Crawford EC; Cooley NR; Schrock E; Ning Y; Ried T
Prenat Diagn; 1998 Nov; 18(11):1174-80. PubMed ID: 9854728
[TBL] [Abstract][Full Text] [Related]
19. De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19.
Cigudosa JC; Odero MD; Calasanz MJ; Solé F; Salido M; Arranz E; Martínez-Ramirez A; Urioste M; Alvarez S; Cervera JV; MacGrogan D; Sanz MA; Nimer SD; Benitez J
Genes Chromosomes Cancer; 2003 Apr; 36(4):406-12. PubMed ID: 12619165
[TBL] [Abstract][Full Text] [Related]
20. Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies.
Skrypnyk C; Goecke TO; Majewski F; Bartsch O
Am J Med Genet; 2002 Nov; 113(2):207-12. PubMed ID: 12407714
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]