First Trimester Quad Screening
FTS
Aneuploidy and pre-eclampsia risk screening.
OnePLUS laboratory & diagnostics
Explore the OnePLUS directory of diagnostic tests and health checkup packages. Find available parameters, sample requirements, and preparation details.
999 available tests & packages
Showing 193–216
FTS
Aneuploidy and pre-eclampsia risk screening.
FISH POC
Rapid detection of common aneuploidies (chromosomes 13, 18, 21, X, Y).
FISH
Rapid detection of common aneuploidies (chromosomes 13, 18, 21, X, Y).
Pre- and post-test counselling; interpretation of genetic results; reproductive options.
Pre- and post-test counselling; interpretation of genetic results; reproductive options.
Alpha Thal MLPA
Molecular diagnosis of alpha / beta thalassaemia; carrier screening and prenatal diagnosis.
HBB
1 listed parameter
Prothrombin gene Mutation
Hereditary Cancer Panel
1 listed parameter
Result
KT+CMA
Copy-number variants beyond karyotype resolution – developmental delay, congenital anomalies, fetal anomalies, miscarriage tissue.
Karyotype NGS
Cause-of-loss analysis in miscarriage / stillbirth; fetal chromosomal assessment.
Karyotype+FISH
Cause-of-loss analysis in miscarriage / stillbirth; fetal chromosomal assessment.
Karyotype
Constitutional chromosome analysis – infertility, recurrent miscarriage, primary amenorrhoea, dysmorphism, ambiguous genitalia.
Karyotype (Couple)
Constitutional chromosome analysis – infertility, recurrent miscarriage, primary amenorrhoea, dysmorphism, ambiguous genitalia.
Prenatal chromosome analysis.
Karyotype POC
Cause-of-loss analysis in miscarriage / stillbirth; fetal chromosomal assessment.
Karyotype POC
Cause-of-loss / aneuploidy testing on products of conception (recurrent miscarriage work-up) or prenatal samples.
CMA 315K
Copy-number variants beyond karyotype resolution – developmental delay, congenital anomalies, fetal anomalies, miscarriage tissue.
CMA 750K
Copy-number variants beyond karyotype resolution – developmental delay, congenital anomalies, fetal anomalies, miscarriage tissue.
CMA POC
Copy-number variants beyond karyotype resolution – developmental delay, congenital anomalies, fetal anomalies, miscarriage tissue.
BWS MLPA
Targeted genetic testing – confirmation of a known or suspected familial variant, carrier screening, prenatal diagnosis.
DMD MLPA
Targeted genetic testing – confirmation of a known or suspected familial variant, carrier screening, prenatal diagnosis.
SMA MLPA
Targeted genetic testing – confirmation of a known or suspected familial variant, carrier screening, prenatal diagnosis.
NBS Extended
Inborn errors of metabolism, endocrine and haemoglobin disorders in newborns.
NBS Panel 7
7 listed parameters
17-OHP, NEONATAL · Biotinidase Neonatal · Cystic Fibrosis , Neonatal