| Non-Cancer Cytogenetic Tests |
| 1p- Microdeletion FISH |
| 4p- Microdeletion FISH |
| 5p- Microdeletion FISH |
| 22q11 microdeletion FISH |
| Amniotic Fluid, Cytogenetics |
| Angelman Syndrome Microdeletion FISH |
| Aneuploidy FISH Panel |
| Blood, Cytogenetics, Constitutional Karyotype |
| Cat Cry Syndrome Microdeletion FISH |
| Cell Culture For Specialty Lab Tests |
| Chorionic Villus Chromosome Analysis |
| Chromosome Analysis, Amniotic Fluid |
| Chromosome Analysis, Blood, Constitutional Karyotype |
| Chromosome Analysis, Chorionic Villus Chromosome Analysis |
| Chromosome Analysis, Percutaneous Umbilical Cord Blood Sample (PUBS) |
| Chromosome Analysis, Solid Tissue, Non-Neoplastic |
| Cri Du Chat Syndrome Microdeletion FISH |
| CVS Chromosome Analysis |
| Cytogenetics, Amniotic Fluid |
| Cytogenetics, Blood, Constitutional Karyotype |
| Cytogenetics, Chorionic Villus Chromosome Analysis |
| Cytogenetics, Percutaneous Umbilical Cord Sample (PUBS) |
| Cytogenetics, Solid Tissue, Non-Neoplastic |
| Deletion Chromosome 1p36 by FISH (1p- Syndrome) |
| Deletion Chromosome 4p16.3 by FISH (4p-) |
| Deletion Chromosome 5p15.2 by FISH (5p-) |
| Deletion Chromosome 7q11.23 by FISH |
| Deletion Chromosome 15q11.2q13 by FISH |
| Deletion Chromosome 17p11.2 by FISH (Smith-Magenis Syndrome) |
| Deletion Chromosome 17p13.3 by FISH (Miller Dieker Syndrome) |
| Deletion Chromosome 22q11.2 by FISH |
| DiGeorge Syndrome Microdeletion FISH |
| Establishment Of Lymphoblastoid Cell Line |
| Fibroblast Culture |
| FISH, 1p- Microdeletion |
| FISH, 4p- Microdeletion |
| FISH, 5p- Microdeletion |
| FISH, 22q11 Microdeletion |
| FISH, Angelman Syndrome |
| FISH, Aneuploidy panel |
| FISH, Chromosome 1 short arm Microdeletion |
| FISH - Constitutional Disorders (non-cancer) |
| FISH, DiGeorge Syndrome Microdeletion |
| FISH, Miller-Dieker Syndrome Microdeletion |
| FISH, Prader-Willi Syndrome Microdeletion |
| FISH, sex chromosomes |
| FISH, Shprintzen Syndrome Microdeletion |
| FISH, Smith-Magenis Syndrome Microdeletion |
| FISH, SRY, Male sex determination |
| FISH, Telomere panel |
| FISH, trisomy panel |
| FISH, Velocardiofacial Syndrome |
| FISH, Williams Syndrome Microdeletion |
| FISH, Wolf-Hirshhorn Syndrome Microdeletion |
| FISH, XY |
| Fluorescence In-Situ Hybridization (FISH), Constitutional Disorders (non-cancer) |
| Freezing Cultured Cells For Future Use |
| Karyotype, Amniotic Fluid |
| Karyotype, Blood, Constitutional Karyotype |
| Karyotype, Chorionic Villus Chromosome Analysis |
| Karyotype, Percutaneous Umbilical Cord Blood Sample (PUBS |
| Karyotype, Solid Tissue, Non-Neoplastic |
| Lymphoblastoid Cell Line, Establishment Of |
| Male sex determination FISH |
| Miller Dieker Syndrome Microdeletion FISH |
| Prader-Willi Syndrome Microdeletion FISH |
| Sex Chromosomes by FISH |
| Shprintzen Syndrome Microdeletion FISH |
| Smith-Magenis Syndrome Microdeletion FISH |
| SRY FISH |
| Subtelomere FISH panel |
| Solid Tissue, Non-Neoplastic, Cytogenetics |
| Telomere FISH panel |
| Trisomy FISH panel |
| Velocardiofacial Syndrome Microdeletion FISH |
| Williams syndrome microdeletion FISH |
| Wolf-Hirschhorn syndrome microdeletion FISH |
| X And Y chromosomes by FISH |
| Cancer Cytogenetic Tests |
| ABL Gene Amplification by FISH (Precursor T-Lymphoblastic Leukemia/Lymphoma) |
| ALK Gene Rearrangement by FISH (Anaplastic Large Cell Lymphoma) |
| Alveolar rhabdomyosarcoma by FISH |
| Anaplastic large cell lymphoma by FISH |
| API2/MALT1 gene rearrangement by FISH (MALT Lymphoma) |
| ATM Gene Deletion by FISH (Chronic Lymphocytic Leukemia) |
| BCL1/IGH Gene Rearrangement by FISH (Mantle Cell Lymphoma) |
| BCL6 Gene Rearrangement by FISH (Diffuse Large B-Cell Lymphoma) |
| BCR/ABL Gene Rearrangement by FISH (Chronic Myelogenous Leukemia, Acute Lymphocyic Leukemia) |
| Blood, Cytogenetics, Suspected Leukemia |
| Bone Marrow, Cytogenetics |
| Burkitt Lymphoma Translocation by FISH |
| Bone Marrow Engraftment by FISH (opposite sex donor) |
| CBFβ Gene Rearrangement by FISH (Acute Myeloid Leukemia, FAB M4eo) |
| CCND1/IGH gene rearrangement by FISH (Mantle Cell Lymphoma) |
| CHIC2 Gene Deletion by FISH (Hypereosinophilic Syndrome) |
| Chromosome 5 Aberrations by FISH (Myelodysplastic Syndrome) |
| Chromosome 7 Aberrations by FISH (Myelodysplastic Syndrome) |
| Chromosome 8 gain by FISH (Multiple Myeloma) |
| Chromosome 12 gain by FISH (Chronic Lymphocytic Leukemia) |
| Chromosome Analysis, Blood, Suspected Leukemia |
| Chromosome Analysis, Bone Marrow |
| Chromosome Analysis, Effusions, Cerebrospinal Fluid |
| Chromosome Analysis, Solid Tumor |
| Chronic Lymphocytic Leukemia (CLL) FISH Panel |
| Chronic Myelogenous Leukemia (CML) FISH (Translocation 9;22) |
| CMYC/IGH gene rearrangement by FISH (Burkitt Lymphoma) |
| Cytogenetics, Blood, Suspected Leukemia |
| Cytogenetics, Bone Marrow |
| Cytogenetics, Effusions, Cerebrospinal Fluid |
| Cytogenetics, Solid Tumor |
| Deletion Chromosome 4q12 by FISH (Hypereosinophilic Syndrome) |
| Deletion Chromosome 7 by FISH (Myelomonocytic Leukemia) |
| Deletion Chromosome 20q by FISH |
| Diffuse large B-cell lymphoma FISH |
| DLBCL FISH |
| Effusions, Cerebrospinal Fluid, Cytogenetics |
| ETO/AML1 Gene Rearrangement by FISH (Acute Myeloid Leukemia, FAB M2) |
| EWSR1 Gene Rearrangement by FISH (Ewing Sarcoma) |
| FISH, 11q23 |
| FISH, ABL1 gene amplification |
| FISH, ALK: (2;5) translocation |
| FISH, API2/MALT1: (11;18) translocation |
| FISH, ATM |
| FISH, BCL1(CCND1)/IGH: (11;14) translocation |
| FISH, BCL6 |
| FISH, BCR/ABL: (9;22) translocation |
| FISH, CBFB: inv(16) |
| FISH, CHIC2 |
| FISH, chromosome 5 aberrations of myelodysplasia |
| FISH, chromosome 7 aberrations of myelodysplasia |
| FISH, CMYC/IGH: (8;14) translocation |
| FISH, deleted 5 |
| FISH, deleted 7 |
| FISH, deletion 4q12 |
| FISH, deletion 20q |
| FISH, deletions in chromosome 5 |
| FISH, deletions in chromosome 7 |
| FISH, ETO/AML1: (8;21) translocation |
| FISH, EWSR1: (11;22) translocation |
| FISH, FKHR: (2;13) translocation |
| FISH, FUS: (12;16) translocation |
| FISH, IGH/BCL2: (14;18) translocation |
| FISH, MLL gene rearrangements |
| FISH, monosomy 7 |
| FISH, MYEOV/IGH |
| FISH - Neoplasic Disorders |
| FISH, NMYC gene amplification |
| FISH, p16 |
| FISH, p53 |
| FISH, PML/RARA: (15;17) translocation |
| FISH, RB1 |
| FISH, Retinoblastoma gene |
| FISH, SYT: (X;18) translocation |
| FISH, TEL/AML1: (12;21) translocation |
| FISH, TP53 |
| FISH, trisomy 4, 10, and 17 |
| FISH, trisomy 8 |
|
FISH, trisomy 12
|
| FKHR Gene Rearrangement by FISH (Alveolar Rhabdomyosarcoma) |
| Fluorescence In-Situ Hybridization (FISH), Neoplasic Disorders |
| Follicular Lymphoma Translocation by FISH |
| FUS Gene Rearrangement by FISH (Myxoid Liposarcoma) |
| Hypereosinophilic Syndrome FISH (Deletion 4q12) |
| IGH/BCL2 gene rearrangement by FISH (Follicular Lymphoma) |
| Inversion Chromosome 16 by FISH (Acute Myeloid Leukemia, FAB M4eo) |
| Karyotype, Blood, Suspected Leukemia |
| Karyotype, Bone Marrow |
| Karyotype, Effusions, Cerebrospinal Fluid |
| Karyotype, Solid Tumor |
| Mantle cell lymphoma FISH |
| Marginal Zone B-cell Lymphoma FISH |
| MALT Lymphoma FISH |
| MDS FISH Panel |
| MLL Gene Rearrangement by FISH (11q23) (Acute Myeloid Leukemia) |
| Monosomy 7 FISH |
| Multiple Myeloma FISH Panel |
| Myelodysplastic Syndrome FISH Panel |
| MYEOV/IGH gene rearrangement by FISH (Mantle cell lymphoma) |
| Myxoid Liposarcoma by FISH |
| Neuroblastoma by FISH |
| NMYC Gene Amplification by FISH (Neuroblastoma) |
| Nodular lymphoma by FISH |
| P16 Gene Rearrangement by FISH (Precursor T-Lymphoblastic Leukemia/Lymphoma) |
| P53 Gene Deletion by FISH (Chronic Lymphocytic Leukemia, Multiple Myeloma) |
| Philadelphia-chromosome translocation by FISH |
| PML/RARA Gene Rearrangement by FISH (Acute Promyelocytic Leukemia) |
| PNET FISH |
| RB1 Gene Deletion by FISH (Chronic Lymphocytic Leukemia, Multiple Myeloma) |
| Sex Chromosomes by FISH |
| Solid Tumor, Cytogenetics |
| Synovial Sarcoma by FISH |
| SYT Gene Rearrangement by FISH (Synovial Sarcoma) |
| TEL/AML1 Gene Rearrangement by FISH (Precursor - B ALL) |
| TP53 Gene Deletion by FISH (Chronic Lymphocytic Leukemia, Multiple Myeloma) |
| Translocation (2;5) by FISH (Anaplastic Large Cell lymphoma) |
| Translocation (8;14) by FISH (Burkitt Lymphoma) |
| Translocation (8;21) by FISH (Acute Myeloid Leukemia, FAB M2) |
| Translocation (9;22) by FISH (Chronic Myelogenous Leukemia, Acute Lymphocyic Leukemia) |
| Translocation (11;14) by FISH (Multiple Myeloma, Mantle Cell Lymphoma) |
| Translocation (11;18) by FISH (Malt Lymphoma) |
| Translocation (12;16) by FISH (Myxoid liposarcoma) |
| Translocation (12;21) by FISH (Precursor - B ALL) |
| Translocation (14;18) by FISH (Follicular Lymphoma) |
| Translocation (15;17) by FISH (Acute Promyelocytic Leukemia) |
| Translocation (16;16) by FISH (AML) |
| Translocation (X;18) by FISH (Synomial Sarcoma) |
| Trisomy Chromosome 3 by FISH (Multiple Myeloma) |
| Trisomy Chromosomes 4, 10 and 17 by FISH (Precursor - B ALL) |
| Trisomy Chromosome 8 by FISH (Multiple Myeloma) |
| Trisomy Chromosome 9 by FISH (Multiple Myeloma) |
| Trisomy Chromosome 12 by FISH (Chronic Lymphocytic Leukemia) |
