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Global Panel
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Cardiovascular Diseases global panel [405 genes] see panel Download form Download informed consent
Cardiomyopathy Panels
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Arrhythmias global panel [251 genes] see panel Download form Download informed consent
Cardiomyopathies global panel [204 genes] see panel Download form Download informed consent
Hypertrophic Cardiomyopathy panels [118 / 18 genes] see panel Download form Download informed consent
Dilated Cardiomyopathy panel [121 genes] see panel Download form Download informed consent
Arrhythmogenic Cardiomyopathy panel [26 genes] see panel Download form Download informed consent
Non compaction Cardiomyopathy panel [48 genes] see panel Download form Download informed consent
Restrictive Cardiomyopathy panel [23 genes] see panel Download form Download informed consent
RASopathies panel [26 genes] see panel Download form Download informed consent
CHANNELOPATHIES–ARRHYTHMIAS panels
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Arrhythmias global panel [251 genes] see panel Download form Download informed consent
Ventricular arrhythmia and sudden death without structural heart disease panel [90 genes] see panel Download form Download informed consent
Long QT syndrome panels [32 / 11 genes] see panel Download form Download informed consent
Short QT syndrome panel [9 genes] see panel Download form Download informed consent
Catecholaminergic polymorphic ventricular tachycardia panel [10 genes] see panel Download form Download informed consent
Brugada syndrome / J wave syndrome panel [27 genes] see panel Download form Download informed consent
Cardiac conduction disease panel [44 genes] see panel Download form Download informed consent
Atrial Fibrillation panel [46 genes] see panel Download form Download informed consent
Aortic diseases global panel
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Aortic diseases global panel [41 genes]:
Marfan / TAAD / Loeys-Dietz / Ehlers-Danlos / Shprintzen-Goldberg
see panel Download form Download informed consent
Congenital Heart diseases panels
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Congenital Heart diseases panel [114 genes] see panel Download form Download informed consent
CNV – SNP ARRAYS STUDY see panel Download form Download informed consent
Dyslipidemias / Early Atherosclerosis panels
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Dyslipidemias / Early Atherosclerosis panel see panel Download form Download informed consent
Familial Hypercholesterolemia panel see panel Download form Download informed consent
Primary hypertriglyceridemia / Polygenic / Familial combined hyperlipidemia panel see panel Download form Download informed consent
Lipodystrophies panel see panel Download form Download informed consent
Hypolipidemias panel see panel Download form Download informed consent
MODY panel see panel Download form Download informed consent
Rare diseases panels
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Pulmonary Hypertension panel [16 genes] see panel Download form Download informed consent
FABRY DISEASE- Massive parallel sequencing method after amplification of [GLA] gene see panel Download form Download informed consent
Familial Transthyretin Amyloidosis [TTR gen] see panel Download form Download informed consent
Hereditary Hemorrhagic Telangiectasia panel [9 genes] see panel Download form Download informed consent
Mitochondrial Genome see panel Download form Download informed consent
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Familial studies
Exome Services
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FASTQ
FASTQ + annotated variants
FASTQ + annotated variants + interpretation [380 genes]
Whole-genome array Services
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Index case evaluated
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Mitochondrial Genome Sequencing
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Mitochondrial DNA analysis
Familial study
INTERPRETATION SERVICES
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Genetic variants report
step1

Download & fill out both documents
Please cover as many fields as possible in both documents

step2

Obtain sample
3 sample types: saliva, peripheral blood or genomic DNA

step3

Pack the sample
Please pack the sample in a way to prevent leakage

step4

Send the sample & the request
Please schedule the delivery for Mon–Thur: 8am – 5pm

step5

Result: the report
Via HIC Client Portal / Certified email

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