Molecular Tests - Genetic Diagnosis Center DR. Cell

Molecular Tests

Dna Fingerprinting
Thrombophilia Panel 5 Mutations
Thrombophilia Panel 12 Mutations
Thrombophilia Panel Single Mutation
Cardiovascular Risk Panel (12 Mutations)
PGS (Single Embryo)
PGD Single Gene Array Analysis
Nipt (Non Invasive Prenatal Testing)
FMF (Familial Mediterranean Fever)
Cystic Fibrosis - CFTR 19 Mutation
Cystic Fibrosis - CFTR Whole Gene Sequence Analysis
Cystic Fibrosis - CFTR Mlpa Deletion Duplication Analysis
Cystic Fibrosis - CFTR-Prenatal
Y Microdeletion
Celiac Disease
Thalassemia Beta
Beta Thalassemia (Hbb Whole Gene) - Mediterranean Anemia from Amniotic Fluid
Beta Thalassemia (Hbb Gene) - Mediterranean Anemia Mutation Known from Amniotic Fluid
Talesemi Alpha
Jak2 Exon 12 Mutation
HLA B 27
HLA B 57
HLA B51
HLA B52
HLA B5
Huntington's Disease
Alpha-1- Antitrypsin Deficiency
Hearing Loss, Digenic Gjb2/Gjb6 + Mitochondrial A1555g (Whole Gene - Sequence Analysis)
Sma - Smn 1-2 Deletion Carrier Analysis
Sma Mlpa
Dmd (Whole Gene Analysis)
Dmd (Mlpa)
Breed Identification
Whole Exome Sequencing (Wes) Test
Microarray
Noonan Syndrome Ptpn11
Hemochromatosis (Hfe Gene) Whole Gene Sequence Analysis
Noonan Syndrome Ptpn11
Mody All Types
Behcet's Disease
MSI (Mise Ca'da)
Phenylketonuria (Pku)-Pah Whole Gene
Hereditary Deafness Panel
Fragile-X Chromosome Analysis
Marfan Syndrome (Fbn1) Panel
Autoinflammatory Panel (Febrile Diseases Panel)
Celiac Genotyping Test
Familial Cardiomyopathy Panel
Long-Qt Cardiology Panel
Familial Cancer Panel
Cfhr2 (Mlpa)
Zttk Syndrome
Glycogen Storage Disease Panel
Lysosomal Storage Diseases Panel
Neurofibromatosis (Nf1 -Nf2) Panel
Retinitis Pigmentosa Panel
Charcot Marie Tooth Panel
Mitochondrial Panel
Yemen Blindness - Deafness Hypopigmentation Syndrome
Zimmermann - Laband Syndrome
Ataxia Autosomal Panel
Congenital Ichthyosis Panel
Aneurysm Panel
Male Infertility Panel
Alport Syndrome Panel
Alzheimer Panel
Dementia Disorder Panel
Gender Disorders Panel

Update Date: 13.05.2022

Editor

Genetic Diagnosis Center Dr. Cell

Genetic Diagnosis Center

The content of the page is for informational purposes only.
Please consult your physician for diagnosis and treatment.

Genetic Diagnosis Services

Our center mainly provides services in the fields of genetic counseling, cytogenetics, molecular cytogenetics and molecular genetics. The problems of our patients who apply to our center, which are thought to have genetic causes, are helped by using up-to-date information and technology.

Cytogenetic Tests
Chromosome disorders form an important category of genetic disease. Cytogenetic tests examine the number and morphology of chromosomes.
Molecular Tests
Diseases that cause deterioration of human health and change the living order are diagnosed and detected through molecular tests.
Molecular Cytogenetic Tests (Fish)
It is a discipline that expands the scope and increases the diagnostic value of routine chromosome analysis with the combined use of molecular biology and cytogenetic techniques.
Cancer Scanning Tests
Diagnosis of cancer at an early stage greatly affects the success of cancer treatment. Many cancer tests are performed in our genetic diagnosis center.

Services