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IARS2

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

IBA57

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

IER3IP1

Microcephaly Panel

IFITM5

Osteogenesis Imperfecta Panel

Prenatal Skeletal Dysplasia Panel

IFT122

Short-Rib Thoracic Dysplasia (SRTD) Panel

IFT172

Comprehensive Brain Malformations Panel

Joubert Syndrome and Related Disorders Panel

Prenatal Joubert Syndrome and Related Disorders Panel

Short-Rib Thoracic Dysplasia (SRTD) Panel

IFT43

Short-Rib Thoracic Dysplasia (SRTD) Panel

IFT80

Short-Rib Thoracic Dysplasia (SRTD) Panel

IGHMBP2

Axonal CMT Panel

CMT Panel

Hereditary Neuropathy Panel

IGHMBP2 Gene Sequencing

Neuromuscular Disorders Panel

IKBKAP

Hereditary Neuropathy Panel

IKBKG (NEMO)

IKBKG (NEMO) Common Deletion (Female)

IKBKG (NEMO) Gene Sequencing

IKBKG (NEMO) Gene Sequencing & Common Del/Dup

IL2RG

B-positive SCID Panel

Comprehensive SCID Panel

IL2RG Gene Sequencing

IL7R

B-positive SCID Panel

Comprehensive SCID Panel

IL7R Gene Sequencing

ILDR1

Hearing Loss Test

ILK

Custom Cardiomyopathy Panel *

Custom Combined Cardiac Panel *

Custom DCM/LVNC Panel *

Cardiomyopathy Panel

Combined Cardiac Panel

DCM/LVNC Panel

IMPDH1

adRP Tier 1

adRP Tier 3

IMPDH1 Gene Sequencing

INF2

Axonal CMT Panel

CMT Panel

Demyelinating CMT Panel

Hereditary Neuropathy Panel

INPP5E

Comprehensive Brain Malformations Panel

Joubert Syndrome and Related Disorders Panel

Prenatal Joubert Syndrome and Related Disorders Panel

IQSEC2

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

IRAK4

IRAK4 Gene Sequencing

IRF6

IRF6 Exon 4 Sequencing

IRF6 Gene Sequencing

ISCA2

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

Progressive External Ophthalmoplegia (PEO)/Optic Atrophy Nuclear Gene Panel

ISCU

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

ISPD

Comprehensive Brain Malformations Panel

Cortical Brain Malformations Panel

Lissencephaly Panel

Neuromuscular Disorders Panel

Prenatal Lissencephaly Panel

Syndromic Congenital Muscular Dystrophy Panel(SCMD)

ITGA3

Epidermolysis Bullosa (EB) XomeDxSlice

ITGA6

Epidermolysis Bullosa (EB) XomeDxSlice

ITGA6 Gene Sequencing

ITGA7

Congenital Myopathies & Muscular Dystrophies Panel

Neuromuscular Disorders Panel

Syndromic Congenital Muscular Dystrophy Panel(SCMD)

ITGB2

ITGB2 Gene Sequencing

ITGB4

Epidermolysis Bullosa (EB) XomeDxSlice

ITGB4 Gene Sequencing

IVD

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Hyperammonemia, Urea Cycle and Transporter Defects Sequencing Panel

IVD Gene Sequencing

IVD Tier 1

IVD Tier 2

Reflex Del/Dup Testing after Hyperammonemia Panel

ÇALIÅžILAN GENLER

*Detaylı bilgi için her bir testin üstüne tıklayınız.

*Bizim yapmadığımız testlerin bazılarını çalıştırdığımız, hepsi sertifikalı ve yetkin, tüm yurt dışı ve yurt içi Laboratuvarlar ile anlaÅŸmalıyız. Fiyat indirimi, doku örneklerinin güvenli bir ÅŸekilde eldesi, gönderim ve takibi, testlerin açıklanması ve hastaya genetik danışmanlığının verilmesi tamamen bize ait sorumluluklardır. 

© Copyright 2023 by Dr. Hakan Ulucan "GEN HEKİMİ"

Cumhuriyet Mah Yıldıray Çınar Sok No:21

Büyükçekmece İstanbul

0212 872 13 96

0533 409 25 45

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