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

Trisomy 21 ◽

Maternal Blood ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Fetal Cells

Rapid comparative genomic hybridization protocol for prenatal diagnosis and its application to aneuploidy screening of human polar bodies

Fertility and Sterility ◽

10.1016/j.fertnstert.2007.07.1320 ◽

2008 ◽

Vol 90 (3) ◽

pp. 488-496 ◽

Cited By ~ 18

Author(s):

C LANDWEHR ◽

M MONTAG ◽

K VANDERVEN ◽

R WEBER

Keyword(s):

Prenatal Diagnosis ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Aneuploidy Screening ◽

Polar Bodies ◽

Hybridization Protocol

Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature

Birth Defects Research Part A Clinical and Molecular Teratology ◽

10.1002/bdra.23213 ◽

2014 ◽

Vol 100 (4) ◽

pp. 284-293 ◽

Cited By ~ 1

Author(s):

Stavros Sifakis ◽

Makarios Eleftheriades ◽

Dimitra Kappou ◽

Roberta Murru ◽

Anastasia Konstantinidou ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Cytogenetic Analysis ◽

Partial Trisomy ◽

Comparative Genomic ◽

Review Of The Literature ◽

Genomic Hybridization ◽

Comparative Genomic Hybridization Array ◽

Molecular Cytogenetic ◽

Fetal Pathology

Predictors for Choosing Array-Comparative Genomic Hybridization for Prenatal Diagnosis

Obstetrics and Gynecology ◽

10.1097/01.aog.0000447445.54916.9b ◽

2014 ◽

Vol 123 ◽

pp. 100S-101S

Author(s):

Steve Rad ◽

Aaron L. Turner ◽

Dalar Ratousi ◽

Paola Aghajanian ◽

John Williams ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Comparative Genomic ◽

Genomic Hybridization

Partial Trisomy 16p (16p12.2→pter) and Partial Monosomy 22q (22q13.31 →qter) Presenting With Fetal Ascites and Ventriculomegaly: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization

Taiwanese Journal of Obstetrics and Gynecology ◽

10.1016/s1028-4559(10)60105-2 ◽

2010 ◽

Vol 49 (4) ◽

pp. 506-512 ◽

Cited By ~ 2

Author(s):

Chih-Ping Chen ◽

Yi-Ning Su ◽

Richard Shih-Hung Young ◽

Fuu-Jen Tsai ◽

Pei-Chen Wu ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Partial Trisomy ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Partial Monosomy

Multiplex ligation-dependent probe amplification and array comparative genomic hybridization analyses for prenatal diagnosis of cytogenomic abnormalities

Molecular Cytogenetics ◽

10.1186/s13039-014-0084-5 ◽

2014 ◽

Vol 7 (1) ◽

Cited By ~ 9

Author(s):

Zhiyong Xu ◽

Qian Geng ◽

Fuwei Luo ◽

Fang Xu ◽

Peining Li ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Dependent Probe

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype

Yearbook of Obstetrics Gynecology and Women s Health ◽

10.1016/s1090-798x(10)79356-5 ◽

2010 ◽

Vol 2010 ◽

pp. 38-39

Author(s):

J.S. Dungan

Keyword(s):

Prenatal Diagnosis ◽

Comparative Genomic ◽

Genomic Hybridization

Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization

Taiwanese Journal of Obstetrics and Gynecology ◽

10.1016/j.tjog.2013.04.023 ◽

2013 ◽

Vol 52 (2) ◽

pp. 278-284 ◽

Cited By ~ 2

Author(s):

Chih-Ping Chen ◽

Yi-Yung Chen ◽

Schu-Rern Chern ◽

Peih-Shan Wu ◽

Jun-Wei Su ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Placental Mosaicism

Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)

Gene ◽

10.1016/j.gene.2011.12.050 ◽

2012 ◽

Vol 495 (2) ◽

pp. 178-182 ◽

Cited By ~ 8

Author(s):

Chia-Cheng Hung ◽

Chia-Hui Lin ◽

Shin-Yu Lin ◽

Jin-Chung Shin ◽

Chien-Nan Lee ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Comparative Genomic Hybridization Array

Array Cgh ◽

De Novo ◽

Comparative Genomic ◽

Genomic Hybridization ◽

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

Journal of Human Genetics ◽

10.1007/s10038-006-0376-7 ◽

2006 ◽

Vol 51 (5) ◽

pp. 412-417 ◽

Cited By ~ 36

Author(s):

Shoko Miura ◽

Kiyonori Miura ◽

Hideaki Masuzaki ◽

Noriko Miyake ◽

Koh-ichiro Yoshiura ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Amniotic Fluid ◽

Microarray Comparative Genomic Hybridization

Chromosome Abnormalities ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Fetal Dna ◽

Cell Free Fetal Dna ◽

Microarray comparative genomic hybridization in prenatal diagnosis: a review

Ultrasound in Obstetrics and Gynecology ◽

10.1002/uog.11180 ◽

2012 ◽

Vol 40 (4) ◽

pp. 385-391 ◽

Cited By ~ 20

Author(s):

S. C. Hillman ◽

D. J. Mcmullan ◽

D. Williams ◽

E. R. Maher ◽

M. D. Kilby

Keyword(s):

Prenatal Diagnosis ◽

Microarray Comparative Genomic Hybridization

Comparative Genomic ◽

Genomic Hybridization ◽