Array CGH
Array CGH and breast cancer
10
Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGH
10
The use of array-CGH in a cohort of Greek children with developmental delay
8
Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams’ syndrome patients in Saudi Arabia
13
Multicolor banding remains an important adjunct to array CGH and conventional karyotyping
9
Array CGH improves detection of mutations in the GALC gene associated with Krabbe disease
9
Selection of competent blastocysts for transfer by combining time-lapse monitoring and array CGH testing for patients undergoing preimplantation genetic screening: a prospective study with sibling oocytes
13
Array-CGH characterization and genotype-phenotype analysis in a patient with a ring chromosome 6
7
Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong
8
The clinical application of array CGH for the detection of chromosomal defects in 20,126 unselected newborns
5
Opening the archives for state of the art tumour genetic research: sample processing for array CGH using decalcified, formalin fixed, paraffin embedded tissue derived DNA samples
11
MLPA for confirmation of array CGH results and determination of inheritance
7
A model based circular binary segmentation algorithm for the analysis of array CGH data
12
Application of Array Based Comparative Genomic Hybridization to Pediatric Neurologic Diseases
7
A prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics
7
Report of Jacobsen syndrome with a mild facial dysmorphism, severe hearing impairment and thrombocytopenia
6
Distal Xq duplication and functional Xq disomy
12
Original Article Correlating array comparative genomic hybridization findings with histology and outcome in spitzoid melanocytic neoplasms
7
Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas
12
A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy – case report and review of the literature
7