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| ARUP Fetal Molecular Tests (as of Nov 2025) | |
|---|---|
| 0051265 | Achondroplasia (FGFR3) 2 Mutations, Fetal |
| 3019566 | Alpha Globin (HBA1 and HBA2) Sequencing and Deletion/Duplication, Fetal |
| 3003656 | Alpha Thalassemia ( HBA1 and HBA2 ) Deletion/Duplication with reflex to Hb Constant Spring, Fetal |
| 3019803 | Angelman Syndrome and Prader-Willi Syndrome by Methylation-Specific MLPA, Fetal |
| 0051415 | Ashkenazi Jewish Diseases, 16 Genes* *fetal testing on cultured cells can be performed for any of the disorders on this panel contact an ARUP genetic counselor when ordering |
| 3004550 | Beta Globin ( HBB ) Sequencing, Fetal |
| 2013662 | Cystic Fibrosis (CFTR) Expanded Variant Panel, Fetal |
| 2011231 | Duchenne/Becker Muscular Dystrophy (DMD) Deletion/Duplication, Fetal |
| 3005869 | Familial Targeted Sequencing, Fetal |
| 2009034 | Fragile X (FMR1) with Reflex to Methylation Analysis, Fetal |
| 0051270 | Galactosemia (GALT) 9 Mutations, Fetal |
| 2001755 | Hemophilia A (F8) 2 Inversions, Fetal |
| 2008863 | Holoprosencephaly Panel, Sequencing and Deletion/Duplication, Fetal |
| 3019937 | Huntington Disease (HD) CAG Repeat Expansion, Fetal |
| 3016676 | Kell K/k (KEL) Antigen Genotyping, Fetal |
| 2010769 | Noonan Spectrum Disorders Panel, Sequencing, Fetal |
| 3016673 | Platelet Antigen Genotyping Panel, Fetal |
| 3016639 | Red Blood Cell Antigen Genotyping, Fetal |
| 3016679 | RhC/c (RHCE) Antigen Genotyping, Fetal |
| 3016640 | RhD Gene (RHD) Copy Number, Fetal |
| 3016682 | RhE/e (RHCE) Antigen Genotyping, Fetal |
| 2012010 | Skeletal Dysplasia Panel, Sequencing and Deletion/Duplication, Fetal |
| 2013444 | Spinal Muscular Atrophy (SMA) Copy Number Analysis, Fetal |
| 3002096 | Tuberous Sclerosis Complex Panel, Sequencing and Deletion/Duplication, Fetal |
