91 related articles for article (PubMed ID: 16683274)
1. Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.
De Gregori M; Ciccone R; Magini P; Pramparo T; Gimelli S; Messa J; Novara F; Vetro A; Rossi E; Maraschio P; Bonaglia MC; Anichini C; Ferrero GB; Silengo M; Fazzi E; Zatterale A; Fischetto R; Previderé C; Belli S; Turci A; Calabrese G; Bernardi F; Meneghelli E; Riegel M; Rocchi M; Guerneri S; Lalatta F; Zelante L; Romano C; Fichera M; Mattina T; Arrigo G; Zollino M; Giglio S; Lonardo F; Bonfante A; Ferlini A; Cifuentes F; Van Esch H; Backx L; Schinzel A; Vermeesch JR; Zuffardi O
J Med Genet; 2007 Dec; 44(12):750-62. PubMed ID: 17766364
[TBL] [Abstract][Full Text] [Related]
2. Complex chromosomal rearrangements.
Patsalis PC
Genet Couns; 2007; 18(1):57-69. PubMed ID: 17515301
[TBL] [Abstract][Full Text] [Related]
3. Identification of complex and cryptic chromosomal rearrangements by optical genome mapping.
Shi S; Huang P; Yan R; Li R
Mol Cytogenet; 2023 Apr; 16(1):5. PubMed ID: 37101225
[TBL] [Abstract][Full Text] [Related]
4. Case report: Optical genome mapping revealed double rearrangements in a male undergoing preimplantation genetic testing.
Ren J; Keqie Y; Li Y; Li L; Luo M; Gao M; Peng C; Chen H; Hu T; Chen X; Liu S
Front Genet; 2023; 14():1132404. PubMed ID: 37065489
[TBL] [Abstract][Full Text] [Related]
5. Identification of a familial complex chromosomal rearrangement by optical genome mapping.
Yang Y; Hao W
Mol Cytogenet; 2022 Sep; 15(1):41. PubMed ID: 36127686
[TBL] [Abstract][Full Text] [Related]
6. A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences.
Trpchevska N; Dimova I; Arabadji T; Milachich T; Angelova S; Dimitrova M; Hristova-Savova M; Andreeva P; Timeva T; Shterev A
J Assist Reprod Genet; 2017 May; 34(5):659-669. PubMed ID: 28236108
[TBL] [Abstract][Full Text] [Related]
7. A rare complex chromosomal rearrangement in an oligospermic male: a case report and review of the Chinese literature.
Chen YJ; Zhang WW; Sun XM; Hu CJ
Asian J Androl; 2014; 16(2):325-6. PubMed ID: 24457837
[No Abstract] [Full Text] [Related]
8. A familial rearrangement(3;5;9) with paternal and maternal transmission leading to a duplication 3p/ deletion 5p infant.
Rivera H; Domínguez MG
Clinics (Sao Paulo); 2012; 67(6):669-72. PubMed ID: 22760908
[No Abstract] [Full Text] [Related]
9. Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndrome.
Roberti MC; Surace C; Digilio MC; D'Elia G; Sirleto P; Capolino R; Lombardo A; Tomaiuolo AC; Petrocchi S; Angioni A
Orphanet J Rare Dis; 2011 Apr; 6():17. PubMed ID: 21504564
[TBL] [Abstract][Full Text] [Related]
10. Complex human chromosomal and genomic rearrangements.
Zhang F; Carvalho CM; Lupski JR
Trends Genet; 2009 Jul; 25(7):298-307. PubMed ID: 19560228
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q).
Mercier S; Fellmann F; Cattin J; Bresson JL
Prenat Diagn; 1996 Nov; 16(11):1046-50. PubMed ID: 8953640
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.
Mechoso B; Vaglio A; Quadrelli A; Mark HF; Huang XL; Milunsky A; Quadrelli R
Fetal Diagn Ther; 2007; 22(4):249-53. PubMed ID: 17369689
[TBL] [Abstract][Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]