Prenatal diagnosis of complex rearrangement of chromosome 21: The significance of interphase and metaphase fluorescence in situ hybridization and comparative genomic hybridization-Reference-Cited by-同舟云学术

Prenatal diagnosis of complex rearrangement of chromosome 21: The significance of interphase and metaphase fluorescence in situ hybridization and comparative genomic hybridization

Published:2013-10-09 Issue:2 Volume:1 Page:50-53
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Namba Akira¹,Nishiyama Miyuki²,Weiser Joseph J³,Wyatt Phillip³,Kimura Machiko¹,Niizawa Rei¹,Miki Akinori¹,Ishihara Osamu¹,Itakura Atsuo¹,Kamei Yoshimasa¹

Affiliation:

1. Department of Obstetrics and Gynecology Saitama Medical University Iruma‐gun Saitama Japan

2. LabCorp Japan Chuo‐ku Tokyo Japan

3. Integrated Genetics Santa Fe New Mexico

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.22

Reference10 articles.

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2. NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21

3. 46, XY, i(21q) identified by maternal serum screening;Meyers C. M.;Md. Med. J.,1997

4. Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescencein situ hybridization (FISH) and maternal serum screening

5. Technical and clinical assessment of fluorescence in situ hybridization: An ACMG/ASHG position statement. I. Technical considerations: Test and Technology Transfer Committee

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