Carrier screening & thalassemia in Mumbai
Plan ahead for pregnancy: find out whether you carry an inherited condition. 35 tests available through Jammu Genetics Hub in Mumbai — open any test to see what it is for, who it is advised for, its sample type and partner-lab price.
Alpha Thalassemia Mutation Analysis
A definitive genetic test for alpha thalassemia — confirms the diagnosis and specific gene deletion/mutation, beyond what a routine HPLC screen shows.
Beta Thalassemia Mutation Analysis
A definitive genetic test for beta thalassemia — confirms the diagnosis and specific gene mutation, important for family planning and genetic counselling.
Carrier Screening — Expanded Panel (NGS)
A much wider carrier screen (hundreds of genes by NGS) for couples planning a pregnancy who want the most thorough check available.
Carrier Screening — Focused Panel
Checks whether you carry (without symptoms yourself) a gene change for common inherited conditions that could affect your children.
Alpha Globin Gene Sequencing-Individual
Alpha Globin Gene Sequencing-Individual is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Alpha Thalassemia Common Mutations- (Individual)
Alpha Thalassemia Common Mutations- (Individual) is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Alpha Thalassemia Triplication By MLPA
Alpha Thalassemia Triplication By MLPA is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
ARMS-PCR For Sickle Cell Anemia
ARMS-PCR For Sickle Cell Anemia is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
ARMS-PCR For β-Thal 5 Common Mutations
ARMS-PCR For β-Thal 5 Common Mutations is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
B- Thalassemia Prenatal Diagnosis- HBB Gene Seq
B- Thalassemia Prenatal Diagnosis- HBB Gene Seq is a prenatal test on amniotic fluid or CVS to find out whether an unborn baby has inherited thalassemia or a sickle-cell disorder from carrier parents.
B-Thalassemia Prenatal Diagnosis - 5 common mutations
B-Thalassemia Prenatal Diagnosis - 5 common mutations is a prenatal test on amniotic fluid or CVS to find out whether an unborn baby has inherited thalassemia or a sickle-cell disorder from…
B-Thalassemia-5 common mutations
B-Thalassemia-5 common mutations is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
B-Thalassemia-5 common mutations(Trio)
B-Thalassemia-5 common mutations(Trio) is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
B-Thalassemia-HBB Gene Seq
B-Thalassemia-HBB Gene Seq is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
B-Thalassemia-HBB Gene Seq(Duo)
B-Thalassemia-HBB Gene Seq(Duo) is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
B-Thalassemia-HBB Gene Seq(Trio)
B-Thalassemia-HBB Gene Seq(Trio) is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Bio7+TMS+Haemoglobinopathy
Bio7+TMS+Haemoglobinopathy is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
CES Carrier Screening Plus
CES Carrier Screening Plus checks whether you carry a changed copy of a gene linked to a serious recessive condition — usually without having any symptoms.
Delta Beta Thalassemia Del/Dup Analysis Individual
Delta Beta Thalassemia Del/Dup Analysis Individual is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Delta-Beta PCR/ HPFH PCR (Individual)
Delta-Beta PCR/ HPFH PCR (Individual) is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Delta-Beta PCR/ HPFH PCR (PND)
Delta-Beta PCR/ HPFH PCR (PND) is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Haemoglobinopathy
Haemoglobinopathy is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
HbA1c (Glycosylated Haemoglobin)
Shows your average blood sugar level over the last 2–3 months — the gold-standard diabetes test.
MLPA for HBB gene - Individual
MLPA for HBB gene - Individual is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Prenatal Alpha Thalassemia Mutation Screening(3 Common Mutation)
Prenatal Alpha Thalassemia Mutation Screening(3 Common Mutation) is a prenatal test on amniotic fluid or CVS to find out whether an unborn baby has inherited thalassemia or a sickle-cell disorder…
Prenatal Diagnosis For HBB MLPA
Prenatal Diagnosis For HBB MLPA is a prenatal test on amniotic fluid or CVS to find out whether an unborn baby has inherited thalassemia or a sickle-cell disorder from carrier parents.
Sanger Sequencing Analysis For β-Thal Mutation
Sanger Sequencing Analysis For β-Thal Mutation is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Sickle Cell/HbE/HbD (One Parent) +B Thal (Other Parent)+Fetus(Sickle/HbE/HbD+Beta thal)
Sickle Cell/HbE/HbD (One Parent) +B Thal (Other Parent)+Fetus(Sickle/HbE/HbD+Beta thal) is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Sickle Cell/HbE/HbD Mutation Analysis
Sickle Cell/HbE/HbD Mutation Analysis is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Sickle Cell/HbE/HbD Mutation Analysis - Trio
Sickle Cell/HbE/HbD Mutation Analysis - Trio is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Sickle Cell/HbE/HbD Prenatal Diagnosis
Sickle Cell/HbE/HbD Prenatal Diagnosis is a prenatal test on amniotic fluid or CVS to find out whether an unborn baby has inherited thalassemia or a sickle-cell disorder from carrier parents.
Thal Screening HPLC
Thal Screening HPLC is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Thalassemia Screening (HPLC)
Screens for thalassemia trait — recommended for couples planning a pregnancy or in early pregnancy.
WES Carrier Screening Plus
WES Carrier Screening Plus checks whether you carry a changed copy of a gene linked to a serious recessive condition — usually without having any symptoms.
α-Thal 3 Common Mutation
α-Thal 3 Common Mutation is a molecular test for inherited blood-haemoglobin disorders such as thalassemia and sickle-cell disease.
Not sure which test you need? Talk to a geneticist.
Jammu Genetics Hub helps patients in Mumbai connect with BGCI-certified geneticists who explain your options, choose the right test, and walk you through your results — so you understand every report and what to do next.