Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization-Reference-Cited by-同舟云学术

Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization

Published:2016-08-08 Issue:1 Volume:9 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Jang Woori,Chae Hyojin,Kim Jiyeon,Son Jung-Ok,Kim Seok Chan,Koo Bo Kyung,Kim Myungshin,Kim Yonggoo,Park In Yang,Sung In Kyung

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-016-0273-5

Reference22 articles.

1. Shaffer L, McGowan-Jordan J, Schmid M. ISCN 2013. An International System for Human Cytogenetic Nomenclature (2013). Basel: Karger; 2013.

2. Liehr T, Claussen U, Starke H. Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res. 2004;107:55–67.

3. Liehr T, Weise A. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Int J Mol Med. 2007;19:719–31.

4. Paoloni-Giacobino A, Morris MA, Dahoun SP. Prenatal supernumerary r(16) chromosome characterized by multiprobe FISH with normal pregnancy outcome. Prenat Diagn. 1998;18:751–2.

5. Woo HY, Cho HJ, Kong SY, Kim HJ, Jeon HB, Kim EC, et al. Marker chromosomes in Korean patients: incidence, identification and diagnostic approach. J Korean Med Sci. 2003;18:773–8.

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X;Genes;2023-01-18

2. Molecular delineation of de novo small supernumerary marker chromosomes in prenatal diagnosis, a retrospective study;Taiwanese Journal of Obstetrics and Gynecology;2023-01

3. Bibliography;Diagnostic Molecular Biology;2023

4. Case Report: How whole-genome sequencing-based cell-free DNA prenatal testing can help identify a marker mhromosome;Frontiers in Genetics;2022-09-26

5. De Novo Mosaic 6p23-p25.3 Tetrasomy Caused by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p Phenotype: A Case Report and Literature Review;Diagnostics;2022-09-24