Mikrogen - Experting Reproductive Genetics
Experting Reproductive Genetics
Mikrogen
About Us
Why Mikrogen?
Mission-Vision
Quality Policy
Gallery
Our Team
Business Partners
Career
PDPA
Accreditation
Medical Tourism
References
Genetic Counseling
Test Guide
Test Requisition Forms
Test Catalog
Whole Exome / Genome Sequencing
Immunology
Prenatal Genetic Tests
Cardiology
Malformation and Retardation Syndromes
Endocrine Diseases
Skeletal, Connective Tissue and Skin Diseases
Andrology
Obstetrics / Infertility
Metabolic Diseases
Oncogenetics / Pharmacogenetics
Hematology – Oncology
Cytogenetics
Neurology / Muscle Diseases
Other
PGT
PGT-A
PGT-M
PGT-SR
Combined PGT
Scientific Studies
Projects
Project Partners
Publications
Contacts
Corporate & Portal Login
CORPORATE LOGIN
LIOS
ALIS
PORTAL LOGIN
Toggle menu
Search Test
Endocrine Diseases
Mikrogen
>
Genetic Tests
>
Endocrine Diseases
Endocrine Diseases
Resistance to Insulin-Like Growth Factor I
Endocrine Diseases
Hypothyroidism THRA GENE
Endocrine Diseases
Congenital Hypothyroidism Type 4
Endocrine Diseases
Pseudohypoparathyroidism Type IB
Endocrine Diseases
HYPOTHYROIDISM, CONGENITAL, NOT RELATED TO GOITR, 2; CHNG2
Endocrine Diseases
DIO1 Sequence Analysis
Endocrine Diseases
Obesity (BMIQ20)
Endocrine Diseases
Obesity Panel (40 Genes)
Endocrine Diseases
Kallmann Syndrome (12 Genes)
Endocrine Diseases
Extended AHUS Panel
Endocrine Diseases
Alagille Syndrome Panel (2 Genes)
Endocrine Diseases
5 Alpha Reductase Deficiency
Endocrine Diseases
Congenital Adrenal Hyperplasia (11B – Hydroxylase deficiency)
Endocrine Diseases
Congenital Adrenal Hyperplasia (21 Hydroxylase Deficiency) MLPA
Endocrine Diseases
Congenital Adrenal Hyperplasia (21 Hydroxylase Deficiency)
Endocrine Diseases
Congenital Adrenal Hyperplasia (17α – Hydroxylase Deficiency)
Endocrine Diseases
Determination of FSH Receptor Gene Polymorphisms
Endocrine Diseases
FSH Beta Mutation Analysis Common Mutation
Endocrine Diseases
Androgen Receptor Polymorphism Whole Gene
Endocrine Diseases
SOX2 Gene Analysis
Endocrine Diseases
SOX9 Gene Analysis
Endocrine Diseases
McCune-Albright Syndrome
Endocrine Diseases
Congenital Glycosylation Defect Type 1q
Endocrine Diseases
Hemochromatosis Type 4
Endocrine Diseases
Rickets is X Linked
Endocrine Diseases
Growth Hormone Deficiency Panel (3 Genes)
Endocrine Diseases
Konjenital Nefrotik Sendromu (Fin Tipi) TGDA
Endocrine Diseases
Bardet Biedl Syndrome Type17
Endocrine Diseases
Pseudohypoaldosteronism Type 1
Endocrine Diseases
Pseudohypoaldosteronism Type 1
Endocrine Diseases
Thyroid Hormone Resistance/Refetoff Syndrome THRB Gene
Endocrine Diseases
Multiple Endocrine Neoplasia Type 1
Endocrine Diseases
Hemachromatosis Panel
Endocrine Diseases
LH Receptor Gene Polymorphism Screening
Endocrine Diseases
Polycystic Kidney Syndrome Panel
Endocrine Diseases
17-Beta Hydroxysteroid Dehydrogenase 3 Deficiency
Endocrine Diseases
Obesity Morbidity Type 2
Endocrine Diseases
Laron Dwarfism
Endocrine Diseases
Autoimmune Polyendocrinopathy Syndrome Type 1
Endocrine Diseases
Bilatural Mavondular Adrenal Hyperplasia
1
2
3
Next page
