The introduction of arrays in prenatal diagnosis: A special challenge

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent

(2012) Wybo Dondorp et al.   HUMAN MUTATION

Genome-wide arrays: Quality criteria and platforms to be used in routine diagnostics

(2012) Joris R. Vermeesch et al.   HUMAN MUTATION

Diagnostic interpretation of array data using public databases and internet sources

(2012) Nicole de Leeuw et al.   HUMAN MUTATION

A Clinical Perspective on Ethical Issues in Genetic Testing

(2011) R. H. Sijmons et al.   Accountability in Research-Policies and Quality Assurance

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype

(2011) G D'Amours et al.   CLINICAL GENETICS

From Karyotyping to Array-CGH in Prenatal Diagnosis

(2011) K.D. Lichtenbelt et al.   CYTOGENETIC AND GENOME RESEARCH

The causality of de novo copy number variants is overestimated

(2011) Joris R Vermeesch et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow

(2011) Malgorzata Srebniak et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Copy-number changes in prenatal diagnosis

(2011) Melissa Strassberg et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities

(2011) Erin B. Kaminsky et al.   GENETICS IN MEDICINE

Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues?

(2011) G. Pichert et al.   JOURNAL OF MEDICAL GENETICS

XX males SRY negative: a confirmed cause of infertility

(2011) A. Vetro et al.   JOURNAL OF MEDICAL GENETICS

S2-Leitlinie Humangenetische Diagnostik

(2011)   Medizinische Genetik

A copy number variation morbidity map of developmental delay

(2011) Gregory M Cooper et al.   NATURE GENETICS

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

(2011) Elisavet A Papageorgiou et al.   NATURE MEDICINE

ASOX9Duplication and Familial 46,XX Developmental Testicular Disorder

(2011) James J. Cox et al.   NEW ENGLAND JOURNAL OF MEDICINE

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

Array technology in prenatal diagnosis

(2011) Orsetta Zuffardi et al.   Seminars in Fetal & Neonatal Medicine

Application of a target array Comparative Genomic Hybridization to prenatal diagnosis

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

Phenotypic variability and genetic susceptibility to genomic disorders

(2010) S. Girirajan et al.   HUMAN MOLECULAR GENETICS

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

Indikationskriterien und Bewertung der Molekularen Karyotypisierung mittels Mikroarray-Analysen für die genetische Diagnostik konstitutioneller DNA-Veränderungen ? Grundlagen zur Einführung der Abrechnung der Molekularen Karyotypisierung mittels Mikroarray-Analyse in den EBM und die GOÄ

(2010)   Medizinische Genetik

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

(2010) Santhosh Girirajan et al.   NATURE GENETICS

Non-invasive prenatal diagnosis by fetal nucleic acid analysis in maternal plasma: the coming of age

(2010) Rossa W.K. Chiu et al.   Seminars in Fetal & Neonatal Medicine

Ethical issues in perinatal genetics

(2010) Frank A. Chervenak et al.   Seminars in Fetal & Neonatal Medicine

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

The IG-DMR and the MEG3-DMR at Human Chromosome 14q32.2: Hierarchical Interaction and Distinct Functional Properties as Imprinting Control Centers

(2010) Masayo Kagami et al.   PLoS Genetics

Origins and functional impact of copy number variation in the human genome

(2009) Donald F. Conrad et al.   NATURE

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

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

(2009) Linda Kleeman et al.   PRENATAL DIAGNOSIS

Private inherited microdeletion/microduplications: Implications in clinical practice

(2008) Maria Antonietta Mencarelli et al.   European Journal of Medical Genetics

Strong association of de novo copy number mutations with sporadic schizophrenia

(2008) Bin Xu et al.   NATURE GENETICS

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

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

Current controversies in prenatal diagnosis 3: for prenatal diagnosis, should we offer less or more than metaphase karyotyping?

(2008) Caroline M. Ogilvie et al.   PRENATAL DIAGNOSIS

High-resolution array genomic hybridization in prenatal diagnosis

(2008) J. M. Friedman   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