Duzen Laboratories Group Genetic Diseases Evaluation Center
Duzen Laboratories Group Genetic Diseases Evaluation Center
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Multisystem Diseases
genetic tests and test panels for detecting genetic variations or mutations associated with multisystem diseases
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A
Alpha-1-Antitrypsin Genotype Determination (M, S, Z Alleles)
ALPORT Syndrome
Angioedema, hereditary, types I and II
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C
CIAS1 Gene Mutations
Cystic Fibrosis (CFTR) Deletion Duplication Analysis
Cystic Fibrosis (CFTR) Whole Gene Sequence Analysis
Cystic Fibrosis, Common Mutations (Exon 4,7,9,10,11) Sequence Analysis
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F
Familial Mediterranean Fever Gene Sequence Analysis
Familial Mediterranean Fever Mutation Analysis
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G
Gilbert Syndrome – UGT1A1 Gene 5 – (TA) Repeat Number
GLUD1 Gene Sequencing
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H
Hemochromatosis
Hemochromatosis (2 mutations)
Hereditary Transthyretin-Related Amyloidosis
HLA-B51
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K
Kartagener Syndrome Primary Ciliary Dyskinesia [CILD1 (DNAI1) Gene DNA Sequence Analysis]
KCNJ11 Gene Sequencing
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L
Lowe Syndrome (OCRL1 Gene)
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M
MC4R Sequencing
MODY2 GCK Gene Sequencing
MODY3 HNF1A Gene Sequencing
MODY5 HNF1B Gene Sequencing
MODY Genetic Panel
MODY Type 1 (HNF4A Gene)
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N
NF1 Deletion/Duplication Analysis
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P
PFIC3 Genetic Analysis
PFIC2 Genetic Analysis
PFIC1 Genetic Analysis
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S
SFTPA2 Sequencing
SFTPC Sequencing
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T
TERC Sequencing
TERT Sequencing
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W
Whole Exome Sequencing (WES)
WILSON ATP7B Sequencing
Wilson Disease Genetic Analysis
WISKOTT-ALDRICH Syndrome (WAS Gene)
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