Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid-Reference-Cited by-同舟云学术

Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid

Published:2006-04-19 Issue:5 Volume:51 Page:412-417
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Miura Shoko,Miura Kiyonori,Masuzaki Hideaki,Miyake Noriko,Yoshiura Koh-ichiro,Sosonkina Nadiya,Harada Naoki,Shimokawa Osamu,Nakayama Daisuke,Yoshimura Shuichiro,Matsumoto Naomichi,Niikawa Norio,Ishimaru Tadayuki

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg200662.pdf

Reference22 articles.

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2. Barrett IJ, Lomax BL, Loukianova T, Tang SS, Lestou VS, Kalousek DK (2001) Comparative genomic hybridization: a new tool for reproductive pathology. Arch Pathol Lab Med 125:81–84

3. Bianchi DW (2000) Fetal cells in the mother: from genetic diagnosis to diseases associated with fetal cell microchimerism. Eur J Obstet Gynecol Reprod Biol 92:103–108

4. Bianchi DW, LeShane ES, Cowan JM (2001) Large amounts of cell-free fetal DNA are present in amniotic fluid. Clin Chem 47:1867–1869

5. Bianchi DW, Lo YM (2001) Fetomaternal cellular and plasma DNA trafficking: the Yin and the Yang. Ann NY Acad Sci 945:119–131

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