Cytogenetics & Chromosomal
DNA Labs India | Diagnostic Tests
Cytogenetics & Chromosomal
Clinical Overview
Sub-category mapping under Genetics & Genomics
| Reviewed by: Dr. Rajesh Kumar, MD Pathology | ISO 9001:2015 Certified Laboratory
This content is for educational purposes only. Always consult a qualified healthcare provider for medical advice.
Tests
Chromofic Karyoarray Test
To identify chromosomal abnormalities, such as aneuploidies, deletions, duplications, and other stru...
Chromosome Analysis (Karyotype) Blood Test
The purpose of chromosome analysis is to identify chromosomal abnormalities or disorders, such as an...
Chromosome Analysis (Karyotype) Couple Blood Test
This test is prescribed to identify structural or numerical chromosomal abnormalities, such as balan...
Chromosome Analysis High Resolution Neonatal Test
The primary purpose of the Chromosome Analysis High Resolution Neonatal Test is to identify chromoso...
Chromultra Chromosome SNP HD Microarray Test
The purpose of this test is to detect changes or abnormalities in chromosomes using SNP microarray t...
Fanconi's Anemia Stress Cytogenetics Test
The purpose of the Fanconi's Anemia Stress Cytogenetics Test is to detect chromosomal abnormalities,...
FISH - 22q Deletion or LSI Di George / VCFS Test
To diagnose genetic disorders related to 22q11.2 deletion, such as DiGeorge syndrome and VCFS, enabl...
FISH - Aneuploidy Detection Products of Conception (POC) Using Chromosomes 13, 18, 21, X & Y Test
The primary purpose of FISH testing on products of conception is to determine whether a chromosomal...
FISH - Microdeletion Detection for Williams Syndrome Test
The primary purpose of the FISH - Microdeletion Detection for Williams Syndrome Test is to confirm o...
FISH - Prenatal Screening Panel Chromosomes 13, 18, 21, X & Y Test
To be used as a prenatal screen, in conjunction with full chromosome analysis, to detect aneuploidy...
FISH - Prader-Willi Syndrome / SNRPN Test
The primary purpose of the FISH - Prader-Willi Syndrome / SNRPN Test is to detect deletions in the S...
Chromosomes 18, X & Y
The purpose of Chromosomes 18, X & Y testing is to detect numerical abnormalities in chromosomes 18,...
Cord Blood For Karyotyping
To detect chromosomal abnormalities in newborns for early diagnosis and management of genetic disord...
Fetal Blood For Karyotyping
To detect chromosomal abnormalities in the developing fetus, such as extra or missing chromosomes, o...
Karyotyping for Detection of Fragile X Syndrome
To detect the presence of the fragile X site on the X chromosome, aiding in the diagnosis of Fragile...
Microarray 315K+ Single Karyotyping (AF/CVS/CB/POC/PB)
To detect chromosomal abnormalities, including microdeletions and microduplications, for diagnosis o...
m-FISH
To detect chromosomal rearrangements, deletions, and duplications for diagnosing genetic disorders s...
Microarray 60K (Peripheral Blood/Cord Blood/Fetal Blood) + Karyotyping
The purpose of Microarray 60K and Karyotyping is to diagnose genetic disorders and chromosomal abnor...
Microarray 60K (POC)+ Single Karyotying
The purpose of this test is to detect chromosomal abnormalities, gene duplications, and deletions th...
Peripheral Blood for Karyotyping (Couple)
The purpose of peripheral blood karyotyping for couples is to identify chromosomal abnormalities tha...
Prader-Willi Syndrome (Karyotyping + FISH)
The purpose of this test is to diagnose Prader-Willi Syndrome by detecting genetic abnormalities on...
Di-George Syndrome (FISH)
The purpose of the DiGeorge Syndrome (FISH) test is to detect a microdeletion in the 22q11.2 region...
Di-George Syndrome (Karyotyping+FISH)
The purpose of this test is to confirm or rule out DiGeorge Syndrome by detecting the 22q11.2 deleti...
FISH for X and Y
The primary purpose of the FISH for X and Y test is to identify abnormalities in the number or struc...