Cytogenetics Test Requisition | Specimen Information | Billing Information | Contact Us | CPT Codes | Print FISH ANALYSIS, PRADER-WILLI SYNDROME Chromosomal Locus: 15q11.2 Pseudonyms: 15q11.2 deletion, SNRPN gene deletion TURNAROUND TIME: 7 to 10
Cytogenetics Test Requisition | Specimen Information | Billing Information | Contact Us | CPT Codes | Print Pseudonyms: ROS1 (6q22), ROS1 Fusion, Lung Cancer, Non-small cell lung cancer, NSCLC, FISH TURNAROUND TIME: 7 to 10 days CPT CODES: 88271X2
Cytogenetics Test Requisition | Specimen Information | Billing Information | Contact Us | CPT Codes | Print FISH ANALYSIS, SMITH-MAGENIS SYNDROME Chromosomal Locus: 17p11.2 Pseudonyms: Smith Magenis syndrome, 17p11.2 deletion, RAI1 gene deletion
Cytogenetics Test Requisition | Specimen Information | Billing Information | Contact Us | CPT Codes | Print FISH ANALYSIS, SRY/X CENTROMERE Chromosomal Locus: Yp11.3 Pseudonyms: Sex Determining Region of Y, Yp deletion, SRY gene deletion TURNAROUND
Cytogenetics Test Requisition | Specimen Information | Billing Information | Contact Us | CPT Codes | Print FISH ANALYSIS, WILLIAMS SYNDROME Chromosomal Locus: 7q11.23 Pseudonyms: Williams-Beuren syndrome, 7q11.23 deletion, Elastin gene deletion
Cytogenetics Test Requisition | Specimen Information | Billing Information | Contact Us | CPT Codes | Print FISH ANALYSIS, WOLF-HIRSCHHORN SYNDROME Chromosomal Locus: 4p16.3 Pseudonyms: 4p16.3 Deletion, Monosomy 4p, Pitt-Rogers-Danks Syndrome
Cytogenetics Test Requisition | Specimen Information | Billing Information | Contact Us | CPT Codes | Print FISH ANALYSIS, X AND Y CHROMOSOMES Pseudonyms: Ambiguous genitalia, Male infertility, Y chromosome translocation, XX Male, Turner syndrome
The Molecular Genetics Laboratory performs testing of multiple genetic diseases, ranging in complexity from single mutation analysis in Achondroplasia to sequencing of the entire Fibrillin gene for Marfan syndrome testing. The laboratory offers
ACHONDROPLASIA ALBRIGHT HEREDITARY OSTEODYSTROPHY (GNAS1) AMYOTROPHIC LATERAL SCLEROSIS (ALS) ANDROGEN INSENSITIVITY SYNDROME ANGELMAN SYNDROME, METHYLATION STUDIES APERT SYNDROME - FGFR2 EXON 8 BLAU SYNDROME (NOD2/CARD15 COMPLETE GENE) BRAF -
Molecular Test Requisition | Specimen Information | Billing Information | Contact Us | CPT Codes | Print Page ACHONDROPLASIA Gene Symbol: FGFR3 Chromosomal Locus: 4p16.3 Protein: Fibroblast growth factor receptor 3 precursor Pseudonyms: ACH