From Karyotyping to Array-CGH in Prenatal Diagnosis

Evolving applications of microarray analysis in prenatal diagnosis

(2011) Melissa S Savage et al.   CURRENT OPINION IN OBSTETRICS & GYNECOLOGY

Determination of fetal chromosome aberrations from fetal DNA in maternal blood: has the challenge finally been met?

(2011) Sinuhe Hahn et al.   EXPERT REVIEWS IN MOLECULAR MEDICINE

Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses

(2011) I.N. Machado et al.   GENETICS AND MOLECULAR RESEARCH

Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21

(2011) Elisavet A Papageorgiou et al.   NATURE MEDICINE

Revisiting the risk for aneuploidy in fetuses with isolated pyelectasis

(2011) Jeanine F. Carbone et al.   PRENATAL DIAGNOSIS

Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?

(2011) The-Hung Bui et al.   PRENATAL DIAGNOSIS

The detection of chromosome anomalies by QF-PCR and residual risks as compared to G-banded analysis

(2011) Marsha D. Speevak et al.   PRENATAL DIAGNOSIS

aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis

(2011) Isabel Filges et al.   PRENATAL DIAGNOSIS

Rapid methods for targeted prenatal diagnosis of common chromosome aneuploidies

(2011) Brigitte H.W. Faas et al.   Seminars in Fetal & Neonatal Medicine

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

(2010) David T. Miller et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Application of a target array Comparative Genomic Hybridization to prenatal diagnosis

(2010) Ji Hyeon Park et al.   BMC Medical Genetics

Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

(2010) Thomas Liehr et al.   CURRENT GENOMICS

Ethical challenges in providing noninvasive prenatal diagnosis

(2010) Peter A Benn et al.   CURRENT OPINION IN OBSTETRICS & GYNECOLOGY

Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization

(2010) Stuart A Scott et al.   GENETICS IN MEDICINE

Non-invasive aneuploidy detection using free fetal DNA and RNA in maternal plasma: recent progress and future possibilities

(2010) A. T. J. I. Go et al.   HUMAN REPRODUCTION UPDATE

Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

(2010) B. H. W. Faas et al.   JOURNAL OF MEDICAL GENETICS

Fetal sex determination using circulating cell-free fetal DNA (ccffDNA) at 11 to 13 weeks of gestation

(2010) Ranjit Akolekar et al.   PRENATAL DIAGNOSIS

Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting

(2010) Idit Maya et al.   PRENATAL DIAGNOSIS

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis

(2010) S. C. Hillman et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

Pregnancy Complicated by Triploidy: A Comparison of the Three Karyotypes

(2009) Dennis McWeeney et al.   AMERICAN JOURNAL OF PERINATOLOGY

Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples

(2009) Björn Menten et al.   BMC Medical Genetics

Digital Fetal Aneuploidy Diagnosis by Next-Generation Sequencing

(2009) K. V. Voelkerding et al.   CLINICAL CHEMISTRY

Diagnosis of miscarriages by molecular karyotyping: Benefits and pitfalls

(2009) Caroline Robberecht et al.   GENETICS IN MEDICINE

High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings

(2009) M Tyreman et al.   JOURNAL OF MEDICAL GENETICS

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

(2009) M. Shinawi et al.   JOURNAL OF MEDICAL GENETICS

ACOG Committee Opinion No. 446: Array Comparative Genomic Hybridization in Prenatal Diagnosis

(2009)   OBSTETRICS AND GYNECOLOGY

Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray

(2009) Justine Coppinger et al.   PRENATAL DIAGNOSIS

Donnai–Barrow syndrome (DBS/FOAR) in a child with a homozygousLRP2mutation due to complete chromosome 2 paternal isodisomy

(2008) Sibel Kantarci et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genomic Medicine in Prenatal Diagnosis

(2008) SARAH T. SOUTH et al.   CLINICAL OBSTETRICS AND GYNECOLOGY

An algorithm for the prenatal detection of chromosome anomalies by QF-PCR and G-banded analysis

(2008) M. D. Speevak et al.   PRENATAL DIAGNOSIS

Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens

(2008) Lisa G. Shaffer et al.   PRENATAL DIAGNOSIS

Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH

(2008) Weimin Bi et al.   PRENATAL DIAGNOSIS

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

(2008) Ignatia B. Van den Veyver et al.   PRENATAL DIAGNOSIS