Test
Growth Hormone 60MINTS
GH 60min
Growth-hormone deficiency (stimulation) or acromegaly (suppression) – dynamic test, book ahead.
OnePLUS laboratory & diagnostics
Tests & Packages
Explore the OnePLUS directory of diagnostic tests and health checkup packages. Find available parameters, sample requirements, and preparation details.
999 available tests & packages
999 matching entries
Showing 169–192
Test
Growth Hormone 90MINTS
GH 90min
Growth-hormone deficiency (stimulation) or acromegaly (suppression) – dynamic test, book ahead.
Test
Growth Hormone Stimulation Test
GH Stim
Growth-hormone deficiency (stimulation) or acromegaly (suppression) – dynamic test, book ahead.
Test
Growth Hormone Suppression by Glucose
GH Suppression
Growth-hormone deficiency (stimulation) or acromegaly (suppression) – dynamic test, book ahead.
Test
IGF Bp3
IGFBP-3
Short stature, GH deficiency, acromegaly.
Test
IGF-1
IGF-1
Short stature, GH deficiency, acromegaly.
Test
Plasma Renin, Direct
Renin
Primary aldosteronism screening (resistant/early hypertension, hypokalaemia).
Test
PTH (Intact)
iPTH
Hyper/hypoparathyroidism; CKD mineral-bone disorder.
Test
VMA 24 Hours Urine
VMA
1 listed parameter
VMA
Test
VMA Random Urine
VMA
1 listed parameter
VMA
Test
2ND Trimester Pre-Eclampsia Screening
PE Screen
Neural tube defect and aneuploidy screening; pre-eclampsia screening.
Test
Beta Thalassemia Mutation Amnio/Cvs
Beta Thal Mutation
Targeted genetic testing – confirmation of a known or suspected familial variant, carrier screening, prenatal diagnosis.
Test
Biotinidase Activity, Quantitative, Blood
Biotinidase
1 listed parameter
BIOTINIDASE, QUANTITATIVE, BLOOD
Test
Carrier Screening for SMA (MLPA)
SMA Screen
Targeted genetic testing – confirmation of a known or suspected familial variant, carrier screening, prenatal diagnosis.
Test
CF Gene Sequencing
CF Gene Seq
Targeted genetic testing – confirmation of a known or suspected familial variant, carrier screening, prenatal diagnosis.
Test
CFTR Mutation
CFTR
Targeted genetic testing – confirmation of a known or suspected familial variant, carrier screening, prenatal diagnosis.
Test
Chromosomal Microarray 750K (Blood)
CMA 750K
1 listed parameter
Vitamin B1 (Thiamin Pyrophosphate)
Test
Clinical Exome Sequencing
CES
2 listed parameters
COMMENT · Nx Gen Clinical Exome Sequencing Thermofisher
Test
DMD Mutation Analysis
DMD
1 listed parameter
DUCHENNE BECKER MUSCULAR DYSTROPHY (DMD BMD) GEN
Test
Double Marker(Dual) + Pre Eclampsia Screening
Double Marker
3 listed parameters
PlGF · PAPP- A · Attachment
Test
Double Marker/Dual Test
Double Marker
29 listed parameters
Attachment · HCG, Free Beta · PAPP- A
Test
eFTS (Enhanced Fts)
eFTS
Aneuploidy and pre-eclampsia risk screening.
Test
Extended NIPT
NIPT Extended
Non-invasive screening for trisomy 21/18/13 and sex-chromosome aneuploidy from maternal blood (≥10 weeks).
Test
Fetal Seq. POC
Cause-of-loss analysis in miscarriage / stillbirth; fetal chromosomal assessment.