| P50 | author | Ioannis Georgiou | Q104618334 |
| P2093 | author name string | Carolina Sismani | |
| | George Koumbaris | |
| | Marios Ioannides | |
| | Christodoulos Christodoulou | |
| | Ioannis Kallikas | |
| | Paola Evangelidou | |
| | Voula Velissariou | |
| | Philippos C. Patsalis | |
| P2860 | cites work | Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification | Q24530153 |
| | Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients | Q24532183 |
| | Global variation in copy number in the human genome | Q24658083 |
| | Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features | Q24675632 |
| | A method for accurate detection of genomic microdeletions using real-time quantitative PCR. | Q25257530 |
| | De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints | Q30445573 |
| | Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases | Q30830662 |
| | Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities | Q33905292 |
| | Accurate and reliable high-throughput detection of copy number variation in the human genome | Q35173713 |
| | Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations | Q35447657 |
| | Prenatal diagnosis by array-CGH. | Q36265171 |
| | Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports | Q36402087 |
| | Copy number variations and clinical cytogenetic diagnosis of constitutional disorders | Q36863518 |
| | Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases | Q36881942 |
| | The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future | Q36957670 |
| | Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives | Q37057760 |
| | Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects | Q37444640 |
| | Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype | Q42117684 |
| | Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray | Q43531050 |
| | A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations | Q48307715 |
| | Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations | Q51888410 |
| | Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization | Q57537925 |
| | Fluorescence in situ hybridization characterization of apparently balanced translocation reveals cryptic complex chromosomal rearrangements with unexpected level of complexity | Q80130915 |
| | Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens | Q81682845 |
| | Array comparative genomic hybridization in prenatal diagnosis: another experience | Q84060497 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | whole genome sequencing | Q2068526 |
| P304 | page(s) | 24 | |
| P577 | publication date | 2010-11-26 | |
| P1433 | published in | Molecular Cytogenetics | Q15761790 |
| P1476 | title | Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations | |
| P478 | volume | 3 | |