1522 |
Custom Sequence Analysis - Prenatal |
1622 |
Prenatal Trio Whole Exome Sequencing |
3200 |
Mitochondrial Respiratory Chain Enzyme Analysis (ETC) - Skeletal Muscle |
3700 |
Mitochondrial DNA Content (qPCR) Analysis - Skeletal Muscle |
3720 |
Mitochondrial DNA Content (qPCR) Analysis - Liver |
4900 |
Global MAPS - Plasma |
4901 |
Global MAPS - Urine |
6099 |
Huntington Disease Repeat Expansion Analysis (Prenatal) |
6100 |
Incontinentia Pigmenti Common Deletion Analysis (Prenatal) |
6105 |
Myotonic Dystrophy Type 1 Repeat Expansion Analysis (Prenatal Diagnosis) |
6351 |
DMD Deletion/Duplication (Prenatal Diagnosis) |
6574 |
FMR1 CGG Repeat Expansion Prenatal Analysis |
8410 |
FISH Analysis - Prenatal Aneuploidy |
8500 |
Chromosome Analysis - Prenatal - Amniotic Fluid with AFP |
8501 |
Alphafetoprotein Analysis - Amniotic Fluid |
8530 |
Chromosome Analysis - Prenatal - Amniotic Fluid |
8540 |
Chromosome Analysis - Prenatal - Amniotic Fluid with ACHE |
8550 |
Alpha-fetoprotein and Acetylcholinesterase Analysis - Amniotic Fluid |
8639 |
Chromosomal Microarray Analysis - Tissue |
8656 |
Targeted Chromosomal Microarray Analysis - Prenatal - Amniotic Fluid |
8657 |
Targeted Chromosomal Microarray Analysis - Prenatal - CVS |
8670 |
Expanded Chromosomal Microarray Analysis - Prenatal - Amniotic Fluid |
8671 |
Expanded Chromosomal Microarray Analysis - Prenatal - CVS |
8672 |
CMA - Targeted and Limited Karyotype - Prenatal - CVS |
8673 |
CMA - Targeted and Limited Karyotype - Prenatal - Amniotic Fluid |
8675 |
CMA-Expanded and Limited Karyotype - Prenatal - Amniotic Fluid |
8676 |
CMA-Expanded and Limited Karyotype - Prenatal - CVS |
8700 |
Chromosome Analysis - Prenatal - CVS |
8940 |
Herpes Simplex Virus 1 & 2 Analysis |
8945 |
Cytomegalovirus (CMV) Analysis |
8950 |
Toxoplasma gondii (TOXO) Analysis |
8955 |
Parvovirus B19 Analysis |
21200 |
PreSeek™ Non-invasive Prenatal Gene Sequencing Screen |
25000 |
Hematology Profile Panel |
25001 |
Hematology Profile Plus Panel |
25002 |
Liquid Trace Hematology Panel |
BG-24001-P12-5 |
Prenatal Noonan Spectrum Disorders/RASopathy Panel |