Tests by Classification Type

NY State Informed Consent Tests

New York State clients are required by New York State regulations to have completed informed-consent forms on file. When ordering the following tests, all NYS clients are required to indicate to Mayo Clinic Laboratories that informed consent has been obtained:

Mayo Test ID Test Name
BPGMM 2,3-Bisphosphoglycerate Mutase, Full Gene Sequencing Analysis, Varies
2OHGP 2-Hydroxyglutaric Aciduria Gene Panel, Varies
CYPZ 21-Hydroxylase Gene (CYP21A2), Full Gene Analysis, Varies
DD22F 22q11.2 Deletion/Duplication, FISH, Varies
3MGAP 3-Methylglutaconic Aciduria Panel, Varies
GAAWR Acid Alpha-Glucosidase Reflex, Leukocytes
GAAW Acid Alpha-Glucosidase, Leukocytes
ASMW Acid Sphingomyelinase, Leukocytes
APGP Acute Porphyria Gene Panel, Varies
AGXTZ AGXT Gene, Full Gene Analysis, Varies
WASQR Alpha Globin Gene Sequencing, Blood
WASEQ Alpha Globin Gene Sequencing, Varies
FUCW Alpha-Fucosidase, Leukocytes
AGABS Alpha-Galactosidase, Blood Spot
AGAW Alpha-Galactosidase, Leukocytes
AGAS Alpha-Galactosidase, Serum
ATHAL Alpha-Globin Gene Analysis, Varies
IDUAW Alpha-L-Iduronidase, Leukocytes
MANN Alpha-Mannosidase, Leukocytes
ANAS Alpha-N-Acetylglucosaminidase, Serum
ALADW Aminolevulinic Acid Dehydratase, Washed Erythrocytes
ALAD Aminolevulinic Acid Dehydratase, Whole Blood
ATNGS Antithrombin Deficiency, SERPINC1 Gene, Next-Generation Sequencing, Varies
APCZ APC Gene, Full Gene Analysis, Varies
APOL1 APOL1 Genotype, Varies
APO1Z Apolipoprotein A-I (APOA1) Gene, Full Gene Analysis, Varies
APO2Z Apolipoprotein A-II (APOA2) Gene, Full Gene Analysis, Varies
APOEG Apolipoprotein E Genotyping, Blood
ARVGP Arrhythmogenic Cardiomyopathy Multi-Gene Panel, Blood
ARSAZ ARSA Gene, Full Gene Analysis, Varies
ARSU Arylsulfatase A, 24 Hour, Urine
ARSAW Arylsulfatase A, Leukocytes
AJPO Ashkenazi Jewish Mutation Analysis Panel Without Cystic Fibrosis, Varies
HHLP AudioloGene Hereditary Hearing Loss Panel, Varies
AUTOP Autoinflammatory Primary Immunodeficiency (PID) Gene Panel, Varies
ARPKZ Autosomal Recessive Polycystic Kidney Disease (ARPKD), Full Gene Analysis, Varies
BCLGP B-Cell Deficiency Primary Immunodeficiency Disorder Panel (34 genes), Next-Generation Sequencing, Varies
BWRS Beckwith-Wiedemann Syndrome/Russell-Silver Syndrome, Molecular Analysis, Varies
WBSEQ Beta Globin Gene Sequencing, Varies
BGAW Beta-Galactosidase, Blood
BGABS Beta-Galactosidase, Blood Spot
BGA Beta-Galactosidase, Leukocytes
WBDDR Beta-Globin Cluster Locus Deletion/Duplication, Blood
WBDD Beta-Globin Cluster Locus, Deletion/Duplication, Varies
WBSQR Beta-Globin Gene Sequencing, Blood
GBAW Beta-Glucosidase, Leukocytes
BTDZ Biotinidase Deficiency, BTD Full Gene Analysis, Varies
BIOTS Biotinidase, Serum
FLCNZ Birt-Hogg-Dube Syndrome, FLCN Full Gene Analysis, Varies
BMPRZ BMPR1A Gene, Full Gene Analysis, Varies
BRGGP Brugada Syndrome Multi-Gene Panel, Blood
BTKS Bruton Tyrosine Kinase (BTK) Genotype, Full Gene Sequence, Blood
C9ORF C9orf72 Hexanucleotide Repeat, Molecular Analysis, Varies
CANP Canavan Disease, ASPA Mutation Analysis, Varies
CARBR Carbamazepine Hypersensitivity Pharmacogenomics, Varies
CPT2Z Carnitine Palmitoyltransferase II Deficiency, Full Gene Analysis, Varies
CACTZ Carnitine-Acylcarnitine Translocase Deficiency, Full Gene Analysis, Varies
CASRZ CASR Gene, Full Gene Analysis, Varies
COMTQ Catechol-O-Methyltransferase (COMT) Genotype, Varies
CDH1Z CDH1 Gene, Full Gene Analysis, Varies
CDKZ CDKN1C Gene, Full Gene Analysis, Varies
CFTRZ CFTR Gene, Full Gene Analysis, Varies
CHLGP Cholestasis Gene Panel, Varies
CMAPC Chromosomal Microarray, Autopsy, Products of Conception, or Stillbirth, Varies
CMAMT Chromosomal Microarray, Autopsy/Products of Conception/Stillbirth, Tissue
CMACB Chromosomal Microarray, Congenital, Blood
CMAP Chromosomal Microarray, Prenatal, Amniotic Fluid/Chorionic Villus Sampling
CHRAF Chromosome Analysis, Amniotic Fluid
CHRCV Chromosome Analysis, Chorionic Villus Sampling
CHRCB Chromosome Analysis, Congenital Disorders, Blood
CHRTI Chromosome Analysis, Skin Biopsy
MITOT Combined Mitochondrial Analysis, Mitochondrial Full Genome and Nuclear Gene Panel, Varies
AHUSP Complement-Mediated Atypical Hemolytic-Uremic Syndrome (aHUS)/Thrombotic Microangiopathy (TMA) Gene Panel, Varies
CCMGP Comprehensive Cardiomyopathy Multi-Gene Panel, Blood
CDGGP Congenital Disorders of Glycosylation Gene Panel, Varies
NGCDA Congenital Dyserythropoietic Anemia Panel, Next-Generation Sequencing, Varies
FIBNG Congenital Fibrinogen Disorders, FGA, FGB, and FGG Genes, Next-Generation Sequencing, Varies
CLADP Congenital Lactic Acidosis Panel, Varies
SCNGP Congenital Neutropenia, Primary Immunodeficiency Disorder Panel (18 genes), Next-Generation Sequencing, Varies
CPOXZ CPOX Gene, Full Gene Analysis, Varies
CGPH Custom Gene Panel, Hereditary, Next-Generation Sequencing, Varies
CFP Cystic Fibrosis Mutation Analysis, 106-Mutation Panel, Varies
CYSGP Cystinuria Gene Panel, Varies
1A2Q Cytochrome P450 1A2 Genotype, Varies
2B6Q Cytochrome P450 2B6 Genotype, Varies
2C19R Cytochrome P450 2C19 Genotype, Varies
2C9QT Cytochrome P450 2C9 Genotype, Varies
2D6Q Cytochrome P450 2D6 Comprehensive Cascade, Varies
3A4Q Cytochrome P450 3A4 Genotype, Varies
3A5Q Cytochrome P450 3A5 Genotype, Varies
DRPL Dentatorubral-Pallidoluysian Atrophy (DRPLA) Gene Analysis, Varies
DPYDQ Dihydropyrimidine Dehydrogenase Genotype, Varies
DPYDG Dihydropyrimidine Dehydrogenase, DPYD Full Gene Sequencing, Varies
DCMGP Dilated Cardiomyopathy Multi-Gene Panel, Next-Generation Sequencing, Blood
DBMD Duchenne/Becker Muscular Dystrophy, DMD Gene, Large Deletion/Duplication Analysis, Varies
EDSGP Ehlers-Danlos Syndrome Panel (12 Genes), Next-Generation Sequencing and Deletion/Duplication Analysis, Varies
ESPAN Epilepsy/Seizure Genetic Panels by Next-Generation Sequencing (NGS), Varies
REVE1 Erythrocytosis Evaluation, Whole Blood
EPOR Erythropoietin Receptor (EPOR) Gene, Exon 8 Sequencing, Whole Blood
F12NG F12 Gene, Next-Generation Sequencing, Varies
F13NG F13A1 and F13B Genes, Next-Generation Sequencing, Varies
F2NGS F2 Gene, Next-Generation Sequencing, Varies
F5NGS F5 Gene, Next-Generation Sequencing, Varies
FABRZ Fabry Disease, Full Gene Analysis, Varies
F5DNA Factor V Leiden (R506Q) Mutation, Blood
F7NGS Factor VII Deficiency, F7 Gene, Next-Generation Sequencing, Varies
F10NG Factor X Deficiency, F10 Gene, Next-Generation Sequencing, Varies
FDP Familial Dysautonomia, Mutation Analysis, IVS20(+6T>C) and R696P, Varies
FHRGP Familial Hypercholesterolemia and Related Disorders Multi-Gene Panel, Next-Generation Sequencing, Varies
FMTT Familial Mutation, Targeted Testing, Varies
FANCP Fanconi Anemia C Mutation Analysis, IVS4(+4)A->T and 322delG, Varies
HFAOP Fatty Acid Oxidation Gene Panel, Varies
FAO Fatty Acid Oxidation Probe Assay, Fibroblast Culture
FBN1B FBN1 Full Gene Sequence, Varies
FECHZ Ferrochelatase (FECH) Gene, Full Gene Analysis, Varies
FGAZ Fibrinogen Alpha-Chain (FGA) Gene, Full Gene Analysis, Varies
PGXQP Focused Pharmacogenomics Panel, Varies
FXS Fragile X Syndrome, Molecular Analysis, Varies
FFRWB Friedreich Ataxia, Frataxin, Quantitative, Blood
FFRBS Friedreich Ataxia, Frataxin, Quantitative, Blood Spot
GFDZ FTCD Gene, Full Gene Analysis, Varies
GALCR Galactocerebrosidase Reflex, Leukocytes
GALCW Galactocerebrosidase, Leukocytes
GALK Galactokinase, Blood
GALTP Galactose-1-Phosphate Uridyltransferase Biochemical Phenotyping, Erythrocytes
GALT Galactose-1-Phosphate Uridyltransferase, Blood
GAL14 Galactosemia Gene Analysis, 14-Mutation Panel, Varies
GCT Galactosemia Reflex, Blood
GALZ Galactosemia, GALT Gene, Full Gene Analysis, Varies
GATA2 GATA-Binding Protein 2 (GATA2), Full Gene, Next-Generation Sequencing, Varies
GBAZ Gaucher Disease, Full Gene Analysis, Varies
GAUP Gaucher Disease, Mutation Analysis, GBA, Varies
GSNZ Gelsolin (GSN) Gene, Full Gene Analysis
G6PDB Glucose-6-Phosphate Dehydrogenase (G6PD) Full Gene Sequencing, Varies
GA2P Glutaric Aciduria Type II Gene Panel, Varies
GSDGP Glycogen Storage Disease Gene Panel, Varies
GNPTZ GNPTAB Gene, Full Gene Analysis, Varies
GRHPZ GRHPR Gene, Full Gene Analysis, Varies
HFE Hemochromatosis HFE Gene Analysis, Blood
HBEL1 Hemoglobin Electrophoresis Evaluation, Blood
HAEV1 Hemolytic Anemia Evaluation, Blood
F8INP Hemophilia A F8 Gene, Intron 1 and 22 Inversion Mutation Analysis, Prenatal
F8INV Hemophilia A F8 Gene, Intron 1 and 22 Inversion Mutation Analysis, Whole Blood
F81P Hemophilia A F8 Gene, Intron 1 Inversion Known Mutation Analysis, Prenatal, Varies
F81B Hemophilia A F8 Gene, Intron 1 Inversion Known Mutation, Whole Blood
F822B Hemophilia A F8 Gene, Intron 22 Inversion Known Mutation, Whole Blood
F822P Hemophilia A F8 Gene, Intron 22 Inversion Mutation Analysis, Prenatal, Varies
F8NGS Hemophilia A, F8 Gene, Next-Generation Sequencing, Varies
F9KMP Hemophilia B, F9 Gene Known Mutation Analysis, Prenatal
FIXKM Hemophilia B, F9 Gene Known Mutation, Whole Blood
NGSF9 Hemophilia B, F9 Gene, Next-Generation Sequencing, Varies
F11NG Hemophilia C, F11 Gene, Next-Generation Sequencing, Varies
COLAB Hereditary Colon Cancer CGH Array
HCRC Hereditary Colon Cancer Multi-Gene Panel, Varies
HEMP Hereditary Erythrocytosis Mutations, Whole Blood
NGHHA Hereditary Hemolytic Anemia Comprehensive Panel, Next-Generation Sequencing, Varies
HHTGP Hereditary Hemorrhagic Telangiectasia Gene Panel, Varies
HPPAN Hereditary Pancreatitis Panel, Varies
NAGW Hexosaminidase A and Total Hexosaminidase, Leukocytes
NAGS Hexosaminidase A and Total Hexosaminidase, Serum
NAGR Hexosaminidase A and Total, Leukocytes/Molecular Reflex, Whole Blood
MUGS Hexosaminidase A, Serum
HL57R HLA-B*57:01 Genotype, Pharmacogenomics, Varies
HL58R HLA-B*5801 Genotype, Allopurinol Hypersensitivity, Varies
HMBSZ HMBS Gene, Full Gene Analysis, Varies
MPS2Z Hunter Syndrome, Full Gene Analysis, Varies
HAD Huntington Disease, Molecular Analysis, Varies
MPS1Z Hurler Syndrome, Full Gene Analysis, Varies
HCMGP Hypertrophic Cardiomyopathy Multi-Gene Panel, Blood
HIF2A Hypoxia-Inducible Factor Alpha (EPAS1/HIF2A) Gene, Exons 9 and 12 Sequencing, Whole Blood
I2SW Iduronate-2-Sulfatase, Blood
I2SBS Iduronate-2-Sulfatase, Blood Spot
IBDGP Inflammatory Bowel Disease Primary Immunodeficiency (PID) Panel, Varies
IL28Q Interleukin 28B (IL28B) Variant (rs12979860), Varies
KCNN4 KCNN4 Full Gene Sequencing, Varies
KETGP Ketone Disorders Gene Panel, Varies
XYMF Known 45,X, Mosaicism Reflex Analysis, FISH, Whole Blood
KD2T Krabbe Disease Second-Tier Newborn Screen, Blood Spot
KRABZ Krabbe Disease, Full Gene Analysis and Large (30 kb) Deletion, Varies
LQTGP Long QT Syndrome Multi-Gene Panel, Blood
LYNCH Lynch Syndrome Panel, Varies
LALB Lysosomal Acid Lipase, Blood
LALBS Lysosomal Acid Lipase, Blood Spot
PLSD Lysosomal and Peroxisomal Storage Disorders Screen, Blood Spot
LSDGP Lysosomal Storage Disease Gene Panel, Varies
LSD6W Lysosomal Storage Disorders, Six-Enzyme Panel, Leukocytes
LYZZ Lysozyme (LYZ) Gene, Full Gene Analysis, Varies
MSUDP Maple Syrup Urine Disease Gene Panel, Varies
MAPTZ MAPT Gene, Sequence Analysis, 7 Exon Screening Panel, Varies
MFRGP Marfan Syndrome and Related Disorders Multi-Gene Panel, Varies
MATCC Maternal Cell Contamination, Molecular Analysis, Varies
MECPZ MECP2 Gene, Full Gene Analysis, Varies
MCADZ Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency Full Gene Analysis, Varies
MEV1 Methemoglobinemia Evaluation, Blood
MHCZ Methylmalonic Aciduria and Homocystinuria, cblC Type, Full Gene Analysis, Varies
MHDZ Methylmalonic Aciduria and Homocystinuria, cblD Type, Full Gene Analysis, Varies
MMAGP Methylmalonic Aciduria Gene Panel, Varies
MPAGP Methylmalonic Aciduria-Propionic Aciduria Combined Gene Panel, Varies
MITOP Mitochondrial Full Genome Analysis, Next-Generation Sequencing (NGS), Varies
MITON Mitochondrial Nuclear Gene Panel by Next-Generation Sequencing (NGS), Varies
MLH1Z MLH1 Gene, Full Gene Analysis, Varies
MLHPB MLH1 Hypermethylation Analysis, Blood
MLYCZ MLYCD Gene, Full Gene Analysis, Varies
MPLVS MPL Exon 10 Mutation Detection, Varies
MSH2Z MSH2 Gene, Full Gene Analysis, Varies
MSH6Z MSH6 Gene, Full Gene Analysis, Varies
SFPAN Mucopolysaccharidosis III, Multi-Gene Panel, Varies
MP3AZ Mucopolysaccharidosis IIIA, Full Gene Analysis, Varies
MP3BZ Mucopolysaccharidosis IIIB, Full Gene Analysis, Varies
MP3CZ Mucopolysaccharidosis IIIC, Full Gene Analysis, Varies
MP3DZ Mucopolysaccharidosis IIID, Full Gene Analysis, Varies
MPS6Z Mucopolysaccharidosis VI, Full Gene Analysis, Varies
SUMFZ Multiple Sulfatase Deficiency, Full Gene Analysis, Varies
MYHZ MUTYH Gene, Full Gene Analysis, Varies
G6SW N-Acetylgalactosamine-6-Sulfatase, Leukocytes
NAT2 N-Acetyltransferase 2 Gene (NAT2), Full Gene Sequence, Whole Blood
NMPAN Neuromuscular Genetic Panels by Next-Generation Sequencing (NGS), Varies
NCLGP Neuronal Ceroid Lipofuscinosis (Batten Disease) Gene Panel, Varies
NADF Newborn Aneuploidy Detection, FISH
NPABZ Niemann-Pick Disease, Types A and B, Full Gene Analysis, Varies
NIEM Niemann-Pick Type C Detection, Fibroblasts
NPCZ Niemann-Pick Type C Disease, Full Gene Analysis, Varies
NSRGP Noonan Syndrome and Related Disorders Multi-Gene Panel, Blood
NPPAN Peripheral Neuropathy Genetic Panels, Next-Generation Sequencing (NGS), Blood
PDGP Peroxisomal Disorder Gene Panel, Varies
PHAGP Phagocytic Primary Immunodeficiency (PID) Gene Panel, Varies
PHEGP Phenylalanine Disorders Gene Panel, Varies
PMMIL Phosphomannomutase and Phosphomannose Isomerase, Leukocytes
PMPDD PMP22 Gene, Large Deletion/Duplication Analysis, Varies
PMS2Z PMS2 Gene, Full Gene Analysis, Varies
PD2T Pompe Disease Second-Tier Newborn Screening, Blood Spot
PDBS Pompe Disease, Blood Spot
GAAZ Pompe Disease, Full Gene Analysis, Varies
PBGDW Porphobilinogen Deaminase, Washed Erythrocytes
PBGD_ Porphobilinogen Deaminase, Whole Blood
PCGP Porphyria Comprehensive Gene Panel, Varies
PMARP Postmortem Arrhythmia Panel, Varies
PMCMP Postmortem Cardiomyopathy Panel, Varies
PMMFR Postmortem Marfan and Related Panel, Varies
PMNSR Postmortem Noonan and Related Panel, Varies
PPOXZ PPOX Gene, Full Gene Analysis, Varies
PWAS Prader-Willi/Angelman Syndrome, Molecular Analysis, Varies
PADF Prenatal Aneuploidy Detection, FISH
PRKSD PRKAR1A Full Gene Sequencing and Deletion/Duplication Analysis, Varies
PRCNG PROCR Gene, Next-Generation Sequencing, Varies
GRNZ Progranulin Gene (GRN), Full Gene Analysis, Varies
PHD2 Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene Sequencing, Whole Blood
FIBDD PROMETHEUS IBD sgi Diagnostic
PCNGS Protein C Deficiency, PROC Gene, Next-Generation Sequencing, Varies
PRSNG Protein S Deficiency, PROS1 Gene, Next-Generation Sequencing, Varies
PTNT Prothrombin G20210A Mutation, Blood
PRSSZ PRSS1 Gene, Full Gene Analysis, Varies
PSYQP Psychotropic Pharmacogenomics Gene Panel, Varies
PTENZ PTEN Gene, Full Gene Analysis, Varies
PDHC Pyruvate Dehydrogenase Complex, Fibroblasts
PKLRG Pyruvate Kinase Liver and Red Blood Cell (PKLR), Full Gene Sequencing and Large Deletion Detection, Varies
NGENZ Red Blood Cell Enzyme Panel, Next-Generation Sequencing, Varies
NGMEM Red Blood Cell Membrane Panel, Next-Generation Sequencing, Varies
RETZ RET Proto-Oncogene, Full Gene Analysis, Varies
HEXBZ Sandhoff Disease, HEXB Gene, Full Gene Analysis, Varies
SDHBZ SDHB Gene, Full Gene Analysis, Varies
SDHP SDHB, SDHC, SDHD Gene Panel, Varies
SDHCZ SDHC Gene, Full Gene Analysis, Varies
SDHDZ SDHD Gene, Full Gene Analysis, Varies
SERPZ SERPINA1 Gene, Full Gene Analysis, Varies
SCDGP Severe Combined Immunodeficiency Panel (63 genes), Next-Generation Sequencing, Varies
SCTF Sex Chromosome Determination, FISH, Tissue
SRYF Sex-Determining Region Y, Yp11.3 Deletion, FISH
SCADZ Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Full Gene Analysis, Varies
FSHDH SHOX, DHPLC
SMADZ SMAD4 Gene, Full Gene Analysis, Varies
DHCRZ Smith Lemli Optiz, DHCR7 Gene, Full Gene Analysis, Varies
SMN1Z SMN1 Gene, Full Gene Analysis, Varies
SLC1Q Solute Carrier Organic Anion Transporter Family Member 1B1 (SLCO1B1) Genotype, Statin, Varies
SMNCS Spinal Muscular Atrophy Carrier Screening, Deletion/Duplication Analysis, Varies
SMNDX Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies
SBULB Spinobulbar Muscular Atrophy (Kennedy Disease), Molecular Analysis, Varies
STKZ STK11 Gene, Full Gene Analysis, Varies
HEXAZ Tay-Sachs Disease, HEXA Gene, Full Gene Analysis, Varies
TSDP Tay-Sachs Disease, HEXA Mutation Analysis, Varies
TELGP Telomere Defects Gene Panel
THEV1 Thalassemia and Hemoglobinopathy Evaluation, Blood and Serum
THBNG THBD Gene, Next-Generation Sequencing, Varies
TPNUQ Thiopurine Methyltransferase (TPMT) and Nudix Hydrolase (NUDT15) Genotyping, Varies
TPMT3 Thiopurine Methyltransferase Activity Profile, Erythrocytes
AATHR Thrombophilia Profile, Plasma and Whole Blood
TP53Z TP53 Gene, Li Fraumeni Syndrome, Full Gene Analysis, Varies
TPPTL Tripeptidyl Peptidase 1 and Palmitoyl-Protein Thioesterase 1, Leukocytes
ATTRZ TTR Gene, Full Gene Analysis, Varies
TYRGP Tyrosine Disorders Gene Panel, Varies
UBE3Z UBE3A Gene, Full Gene Analysis, Varies
UGTFG UDP-Glucuronosyl Transferase 1A1 (UGT1A1), Full Gene Sequencing, Varies
U1A1Q UDP-Glucuronosyl Transferase 1A1 TA Repeat Genotype, UGT1A1, Varies
UNIPD Uniparental Disomy, Varies
UCDP Urea Cycle Disorders Gene Panel, Varies
GALE Uridine Diphosphate--Galactose 4' Epimerase, Blood
UPGDW Uroporphyrinogen Decarboxylase, Washed Erythrocytes
UPGD Uroporphyrinogen Decarboxylase, Whole Blood
UPGC Uroporphyrinogen III Synthase (Co-Synthase), Erythrocytes
VLCZ Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Full Gene Analysis, Varies
VHLE VHL Gene, Erythrocytosis, Mutation Analysis, Varies
VHLZ VHL Gene, Full Gene Analysis, Varies
VWFNG von Willebrand Disease, VWF Gene, Next-Generation Sequencing, Varies
WARSQ Warfarin Response Genotype, Varies
WS7F Williams Syndrome, 7q11.23 Deletion, FISH, Varies
WDZ Wilson Disease, Full Gene Analysis, Varies
XALDZ X-Linked Adrenoleukodystrophy, Full Gene Analysis, Varies
YMCRO Y Chromosome Microdeletions, Molecular Detection, Varies
MULT Zygosity Testing (Multiple Births), Varies