Prenatal diagnosis of a partial trisomy 13q (q14→qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization

Partial Trisomy ◽

Comparative Genomic ◽

Spectral Karyotyping ◽

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

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

Partial Trisomy 10q (10q25.1 →qter) and Partial Monosomy 13q (13q34→qter) Presenting With Fetal Pyelectasis: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization

10.1016/s1028-4559(10)60116-7 ◽

2010 ◽

Vol 49 (4) ◽

pp. 539-543 ◽

Cited By ~ 6

Author(s):

Chih-Ping Chen ◽

Yi-Ning Su ◽

Fuu-Jen Tsai ◽

Schu-Rern Chern ◽

Chin-Yuan Hsu ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Partial Trisomy ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Partial Monosomy

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

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

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

Partial monosomy 13q (13q21.32→qter) and partial trisomy 8p (8p12→pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization

10.1016/j.tjog.2010.04.001 ◽

2011 ◽

Vol 50 (2) ◽

pp. 205-211 ◽

Cited By ~ 5

Author(s):

Chih-Ping Chen ◽

Yi-Ning Su ◽

Fuu-Jen Tsai ◽

Ming-Huei Lin ◽

Pei-Chen Wu ◽

...

Keyword(s):

Partial Trisomy ◽

Nuchal Translucency ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Partial Monosomy ◽

Increased Nuchal Translucency

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 ◽

Retrospectively investigating the 12-year experience of prenatal diagnosis of small supernumerary marker chromosomes through array comparative genomic hybridization

10.1016/j.tjog.2018.11.026 ◽

2019 ◽

Vol 58 (1) ◽

pp. 139-144

Author(s):

Min-Hui Huang ◽

Cagge Lee ◽

Jia-Shyuhn Chang ◽

Han-Chow Wang ◽

Hui-Ling Lai ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Marker Chromosomes ◽

Small Supernumerary Marker Chromosomes ◽

Supernumerary Marker Chromosomes