150 related articles for article (PubMed ID: 35590339)
1. Analysis of complex chromosomal rearrangements using a combination of current molecular cytogenetic techniques.
He P; Wei X; Xu Y; Huang J; Tang N; Yan T; Yang C; Lu K
Mol Cytogenet; 2022 May; 15(1):20. PubMed ID: 35590339
[TBL] [Abstract][Full Text] [Related]
2. Identification of a balanced complex chromosomal rearrangement involving chromosomes 3, 18 and 21 with recurrent abortion: case report.
Liao Y; Wang L; Zhang D; Liu C
Mol Cytogenet; 2014; 7():39. PubMed ID: 24959204
[TBL] [Abstract][Full Text] [Related]
3. Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies.
Tan YQ; Tan YQ; Cheng DH
Mol Cytogenet; 2020; 13():15. PubMed ID: 32391085
[TBL] [Abstract][Full Text] [Related]
4. Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations.
Liang D; Wang Y; Ji X; Hu H; Zhang J; Meng L; Lin Y; Ma D; Jiang T; Jiang H; Asan ; Song L; Guo J; Hu P; Xu Z
Clin Genet; 2017 Apr; 91(4):605-610. PubMed ID: 27491356
[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. Accurate Identification of Breakpoints in a Cryptic Reciprocal Translocation by Whole-Genome Sequencing.
Chen J; Lyu GZ; Jiang F; Zhang VW; Li DZ
Cytogenet Genome Res; 2022; 162(7):386-390. PubMed ID: 36893740
[TBL] [Abstract][Full Text] [Related]
7. A case with balanced chromosome rearrangement involving chromosomes 9, 14, and 13 in a woman with recurrent abortion.
Kim SK; Kim HJ; Yang YH; Kim IK; Bai SW; Kim JY; Park KH; Cho DJ; Song CH
Yonsei Med J; 2001 Jun; 42(3):345-8. PubMed ID: 11456402
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Analysis of cytogenetic characteristics and fertility of carriers of complex chromosomal rearrangements from Henan region].
Dai P; Gao S; Hou Y; Kong X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Feb; 36(2):161-164. PubMed ID: 30703238
[TBL] [Abstract][Full Text] [Related]
10. A de novo complex chromosome rearrangement associated with multisystematic abnormalities, a case report.
Tian C; Li D; Liu P; Jiao L; Gao X; Qiao J
Mol Cytogenet; 2017; 10():32. PubMed ID: 28878823
[TBL] [Abstract][Full Text] [Related]
11. A complex chromosome rearrangement involving chromosome 8, 11, and 12 analyzed by conventional cytogenetic investigations, fluorescence in situ hybridisation, and spectral karyotyping.
Kotzot D; Holland H; Köhler M; Froster UG
Ann Genet; 2001; 44(3):135-8. PubMed ID: 11694225
[TBL] [Abstract][Full Text] [Related]
12. Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report.
de Vree PJ; Simon ME; van Dooren MF; Stoevelaar GH; Hilkmann JT; Rongen MA; Huijbregts GC; Verkerk AJ; Poddighe PJ
Mol Cytogenet; 2009 Jul; 2():15. PubMed ID: 19594915
[TBL] [Abstract][Full Text] [Related]
13. Two cases of mosaicism for complex chromosome rearrangements (CCRM) associated with secondary infertility.
Lebbar A; Callier P; Baverel F; Marle N; Patrat C; Le Tessier D; Mugneret F; Dupont JM
Am J Med Genet A; 2008 Oct; 146A(20):2651-6. PubMed ID: 18798330
[TBL] [Abstract][Full Text] [Related]
14. SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq).
Johnson SH; Smadbeck JB; Smoley SA; Gaitatzes A; Murphy SJ; Harris FR; Drucker TM; Zenka RM; Pitel BA; Rowsey RA; Hoppman NL; Aypar U; Sukov WR; Jenkins RB; Feldman AL; Kearney HM; Vasmatzis G
Cancer Genet; 2018 Feb; 221():1-18. PubMed ID: 29405991
[TBL] [Abstract][Full Text] [Related]
15. Analysis of chromosomal structural variations in patients with recurrent spontaneous abortion using optical genome mapping.
Rao H; Zhang H; Zou Y; Ma P; Huang T; Yuan H; Zhou J; Lu W; Li Q; Huang S; Liu Y; Yang B
Front Genet; 2023; 14():1248755. PubMed ID: 37732322
[No Abstract] [Full Text] [Related]
16. De novo exceptional complex chromosomal rearrangement in a healthy fertile male: case report and review of the literature.
Farra C; Singer S; Dufke A; Ashkar H; Monsef C; Awwad J
Fertil Steril; 2011 Nov; 96(5):1160-4. PubMed ID: 21851937
[TBL] [Abstract][Full Text] [Related]
17. [Molecular cytogenetic analysis for a familial complex chromosomal rearrangement].
Qian WP; Tan YQ; Tjia WM; Song D; Guan XY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):302-4. PubMed ID: 15952121
[TBL] [Abstract][Full Text] [Related]
18. Assessment of molecular cytogenetic methods for the detection of chromosomal abnormalities.
Une T; Yokoyama Y; Ninomiya S; Shinozuka M; Maruyama H; Morishima T
Acta Med Okayama; 2006 Oct; 60(5):279-87. PubMed ID: 17072374
[TBL] [Abstract][Full Text] [Related]
19. A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing.
Hochstenbach R; van Binsbergen E; Schuring-Blom H; Buijs A; Ploos van Amstel HK
Eur J Med Genet; 2019 Sep; 62(9):103543. PubMed ID: 30248410
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
