Prenatal Diagnosis of Trisomy 21 with Fetal Cells in Maternal Blood Using Comparative Genomic Hybridization

Objective: This study was undertaken to determine the clinical use of comparative genomic hybridization (CGH) for detection of fetal trisomy 21 from fetal ceIls (nucleated red blood cells; nRBCs) isolated from maternal peripheral venous blood. Methods: Maternal peripheral venous blood samples were c...

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Veröffentlicht in:	Fetal diagnosis and therapy 2006-01, Vol.21 (1), p.125-133
Hauptverfasser:	Yang, Young Ho, Yang, Eun Suk, Kwon, Ja Young, Kim, In Kyu, Park, Yong Won
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Chromosome aberrations DNA - analysis Down Syndrome - diagnosis Down Syndrome - embryology Down Syndrome - genetics Erythrocytes - cytology Female Fetus - cytology Gynecology. Andrology. Obstetrics Humans Male Management. Prenatal diagnosis Medical genetics Medical sciences Nucleic Acid Hybridization - methods Placental Circulation Pregnancy Pregnancy. Fetus. Placenta Prenatal Diagnosis
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