Genetik, Epigenetik, Bütüncül Tıp, GETAT, Wellness

ESTETIK INTERNATIONAL
Gen Sağlığı-Wellness-Geleneksel ve Tamamlayıcı Tıp
ÇALIŞILAN 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 anlaşmalıyız. Fiyat indirimi, doku örneklerinin güvenli bir şekilde eldesi, gönderim ve takibi, testlerin açıklanması ve hastaya genetik danışmanlığının verilmesi tamamen bize ait sorumluluklardır.
R
RAB18
Comprehensive Brain Malformations Panel
Cortical Brain Malformations Panel
RAB3GAP1
Comprehensive Brain Malformations Panel
Cortical Brain Malformations Panel
RAB3GAP2
Comprehensive Brain Malformations Panel
Cortical Brain Malformations Panel
RAB7A
RAC2
RAD21
Cornelia de Lange Syndrome Panel
RAD51C
RAD51D
RAF1
Custom Combined Cardiac Panel *
Prenatal Noonan Spectrum Disorders Panel
RAG1
RAG2
RAI1
RAI1 Gene Sequencing & Del/Dup
RANBP2
Combined Mito Genome Plus Mito Nuclear Gene Panel
Comprehensive Mitochondrial Nuclear Gene Panel
Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel
RANGRF
Custom Combined Cardiac Panel *
RAPSN
Congenital Myasthenia Syndromes Panel
RARS
Combined Mito Genome Plus Mito Nuclear Gene Panel
Comprehensive Mitochondrial Nuclear Gene Panel
RARS2
Combined Mito Genome Plus Mito Nuclear Gene Panel
Comprehensive Brain Malformations Panel
Comprehensive Mitochondrial Nuclear Gene Panel
Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel
Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel
Pontocerebellar Hypoplasia Panel
Prenatal Pontocerebellar Panel
RASA1
Hereditary Hemorrhagic Telangiectasia Panel
RAX
RB1
RBBP8
RBM20
Custom Combined Cardiac Panel *
RDH5
RDS (PRPH2)
Cone-Rod Dystrophy Sequencing Panel
RDX
REEP1 (C2ORF23)
Combined Mito Genome Plus Mito Nuclear Gene Panel
Comprehensive Hereditary Spastic Paraplegia Panel
Comprehensive Mitochondrial Nuclear Gene Panel
Uncomplicated Hereditary Spastic Paraplegia Panel
RELN
Comprehensive Brain Malformations Panel
Cortical Brain Malformations Panel
Pontocerebellar Hypoplasia Panel
Prenatal Pontocerebellar Panel
RET
PGL/PCC (Paraganglioma/Pheochromocytoma) Panel
RET Remaining Exons Sequencing (HSCR)
RET Remaining Exons Sequencing (MEN2A & MEN2B)
RET Remaining Exons Sequencing (MEN2A)
RET Remaining Exons Sequencing (MEN2B)
RET Select Exons Sequencing (HSCR)
RET Select Exons Sequencing (MEN2A)
RET Select Exons Sequencing (MEN2B)
RFT1
Combined Mito Genome Plus Mito Nuclear Gene Panel
Comprehensive Mitochondrial Nuclear Gene Panel
RHO
RIN2
RIT1
Custom Combined Cardiac Panel *
Prenatal Noonan Spectrum Disorders Panel
RLBP1
RMND1
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
RMRP
RNASEH2A
RNASEH2B
RNASEH2C
RP1
RP2
RPE65
RPGRIP1
RPGRIP1L
Comprehensive Brain Malformations Panel
Joubert Syndrome and Related Disorders Panel
Prenatal Joubert Syndrome and Related Disorders Panel
RPL11
RPL15
RPL26
RPL35A
RPL5
RPS10
RPS17
RPS19
RPS24
RPS26
RPS29
RPS7
RRM2B
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
Progressive External Ophthalmoplegia (PEO)/Optic Atrophy Nuclear Gene Panel
RSK2
RSK2 (RPS6KA3) Gene Sequencing
RSK2 (RPS6KA3) Gene Sequencing & Del/Dup
RSK2 (RPS6KA3) Remaining Exons Sequencing
RSK2 (RPS6KA3) Select Exons Sequencing
RTN2
Comprehensive Hereditary Spastic Paraplegia Panel
Uncomplicated Hereditary Spastic Paraplegia Panel
RTTN
Comprehensive Brain Malformations Panel
Cortical Brain Malformations Panel
RYR1
Congenital Myopathies & Muscular Dystrophies Panel
Reflex Del/Dup Testing After Metabolic Myopathy
RYR2