Cytogenetic Diagnosis

Showing all 17 results

DiseaseModalityDeliveryReferenceData sheet
Genomic array (CNV + SNPs), postnatalArray CytoScan 750K35 daysLV3490
Genomic array (CNV + SNPs), postnatalArray CytoScan HD35 daysLV3489
Genomic array (CNV + SNPs), postnatalClinical Interpretation of arrays42 daysLV2409
FISH (Fluorescence In Situ Hybridization)Detection Down/Patau Syndrome2 daysLV2148
FISH (Fluorescence In Situ Hybridization)Detection Edwards/sex chromosomal syndromes2 daysLV2149
FISH (Fluorescence In Situ Hybridization)Detection of microdeletion syndromes21 daysLV1345
FISH (Fluorescence In Situ Hybridization)Identification of satellited supernumerary marker chromosomes21 daysLV3294
Karyotype, Peripheral Blood Chromosome AnalysisKaryotype in Peripheral Blood. 550 bands. Urgent deadline14 daysLV0455
Karyotype, Peripheral Blood Chromosome AnalysisKaryotype in Peripheral Blood.550-850 bands (high-resolution)28 daysLV0450
Screening in maternal bloodNon-invasive prenatal testing for fetal aneuploidies of chromosomes 13, 18, 21.BabyTest7 daysLV3470
Screening in maternal bloodNon-invasive prenatal testing for fetal aneuploidy (all chromosomes). BabyTest Plus7 daysLV2883
Screening in maternal bloodNon-invasive prenatal testing of fetal chromosomal aneuploidies and CNVs in maternal blood. SG BabyTest Advanced7 daysLV3779
FISH (Fluorescence In Situ Hybridization)Rearrangements of genes or regions21 daysLV1077
Screening in maternal bloodRhD detection in maternal blood3 daysLV2671
FISH (Fluorescence In Situ Hybridization)Screening of aneuploidies (13, 18, 21, X e Y) in peripheral blood2 daysLV2147
Screening in maternal bloodSex fetal detection in maternal blood3 daysLV2667
FISH (Fluorescence In Situ Hybridization)Specific chromosome aneuploidy detection2 daysLV2373