Clinical Genetics - Prenatal
Studies in Clinical Genetics
| CODE | STUDY |
|---|---|
| GC001 | Whole Exome Sequencing (WES) |
| GC002 | Whole Exome Sequencing plus CNVs (copy number variation). |
| GC044 | Whole Exome Sequencing plus bioinformatics CNVs (copy number variation) plus mitochondrial genome (25X) |
| GC003 | Customized NGS Sequencing Panel (according to the clinical picture) |
| GC004 | Targeted Exome Sequencing, TRIO |
| GC005 | Targeted Exome Sequencing plus Mitochondrial Genome |
| GC006 | Mitochondrial Genome Sequencing |
| GC007 | Whole Exome Sequencing plus Molecular Karyotyping (aCGH 180K |
| GC008 | Genetic Checkup PLUS |
| GC009 | Epilepsies Panel plus ADNFarma |
| GC010 | Genetic metabolic screening / Includes ADNfarma study |
| GC011 | Genetic Autism Study |
| GC012 | Immune Panel |
| GC046 | Clinical Exome ADNfarma ADNLIFE |
| GC013 | Sequencing of 1 to 15 genes |
| GC014 | Sequencing for Rett Syndrome |
| GC015 | Sequencing for Marfan Syndrome |
| GC016 | Sequencing of Duchenne and Becker muscular dystrophy |
| GC017 | Duchenne and Becker muscular dystrophy |
| GC018 | Duchenne and Becker muscular dystrophy |
| GC019 | Bone Dysplasia Panel |
| GC020 | Sequencing for Charcot–Marie–Tooth |
| GC021 | Huntington's chorea |
| GC022 | Y chromosome microdeletions |
| GC023 | Fragile X syndrome |
| GC024 | Cystic Fibrosis Disease |
| GC025 | Cystic Fibrosis Disease by Sequencing |
| GC026 | Genetic carrier panel |
| GC027 | DUO genetic carrier panel |
If you require further information, please do not hesitate to contact us.
It will be a pleasure to talk to you and give you more details.
