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Requisitions forms »

A

ABL Kinase mutation and Gleevec® resistance»

Acute lymphoblastic leukemia (Adult) profile includes:

BCR/ABL 9q34 t(9;22), MLL 11q23, MYB del6q, TEL/AML1 ES t(12;21)

Acute Lymphoblastic Leukemia (Pediatric) profile includes:

BCR/ABL 9q34 t(9;22), MLL 11q23, +4, +10, TEL/AML1 ES t(12;21)

ALK 2p23 anaplastic large cell lymphoma by FISH
Alphafetoprotein (amniotic fluid and maternal serum)
AML 1ETO t(8;21) AML by FISH»
API2/MALT1 t(11;18) MALT lymphoma by FISH
ATM deletion 11q22.3 chronic lymphocytic leukemia by FISH
AneuVysion: +13/+18/+21 / X / Y by FISH
Angelman syndrome del 15q11q13 by FISH
ASS deletion 9q34 by FISH
ATM deletion 11q22.3 chronic lymphocytic leukemia by FISH

 

B

B-cell Immunoglobulin Heavy Chain gene rearrangement by PCR »
(BCL1) IGH/CCND1 t(11;14) mantle cell lymphoma by FISH »
(BCL2) IGH/BCL2 t(14;18) follicular lymphoma by FISH »
BCL2 t(14;18) gene rearrangement by PCR »
BCL6 3q27 B-cell non-Hodgkin lymphoma by FISH
BCR/ABL 9q34 t(9;22) philadelphia chromosome by FISH »
BCR/ABL t(9;22) major p210 and minor p190 quantitative by PCR
BCR/ABL major t(9;22) p210 by quantitative PCR »
BCR/ABL minor t(9;22) p190 by quantitative PCR »
Bone marrow pathology examination »
Breast markers:

CellSearch™ circulating tumor cell test
Cytokeratin 5, p63, CK8/18 cocktail by IHC
Cathepsin D by IHC
Cell cycle analysis; DNA Ploidy and S Phase by flow cytometry
E-Cadherin epithelial cell, ductal-type by IHC
Estrogen/Progesterone receptors by IHC»
Gross cystic disease fluid protein 15 (BRST-2 protein) by IHC
Herceptest (Her2/neu) by IHC»
HER2/neu PathVysion®, by FISH»
Ki67 by IHC»
p53 by IHC

Breast 2 profile by IHC:

Cytokeratin 5, p63, CK8/18 breast cocktail double stain by IHC

Bronchoalveolar lavage (CD3, CD4, CD8, CD16, CD4:CD8 ratio) by flow cytometry

C

Cancer antigen 15-3
Cancer antigen 19-9
Cancer antigen 125
Carcinoembryonic antigen
CellSearch™ circulating tumor cell test for metastic cancer: breast, colon, prostate »
CBFB t(16;16), inv(16) AML with eosinophilia by FISH »
Cell cycle analysis; DNA Ploidy and S Phase by flow cytometry
CBFB t(16;16), inv(16) AML by FISH
CD4 and T-cell subsets (CD3, CD4, CD8, CD4:CD8) by flow cytometry
Cell cycle analysis; DNA Ploidy and S Phase by flow cytometry
CEP 7 -7/del 7q31 AML, MDS by FISH »
Chlamydia Trachomatis, Qualitative by Aptima COMBO® 2 TMA
Chromosome analysis (Cytogenetics)

Cancer:

Bone marrow »

Unstimulated peripheral blood »

Constituional:

Peripheral blood »

Prenatal amniotic fluid »

Chorionic villus Products of conception, Solid tissue »

Chronic lymphocytic leukemia profile by FISH includes:

p53 del 17p13.1, ATM del 11q22.3, del 13q14.3 / del 13q34, +12, MYB del 6q

Chronic myeloproliferative disorder by FISH: BCR/ABL 9q34 t(9;22)
C MYC 8q24 Burkitt lymphoma, B-cell large lymphoma by FISH
C MYC 8q24 breast, prostate and other solid tumor by FISH
Comprehensive Leukemia/and or Lymphoma evaluation by flow cytometry
Cri-du-Chat syndrome deletion 5p15.2 by FISH
Cystic Fibrosis 32 mutation analysis panel by PCR (diagnostic, carrier) »

Cystic Fibrosis 32 mutation analysis panel by PCR( prenatal)»
Cystic Fibrosis Intron 8 5T/7T/9T by PCR»

D

deletion 13q14.3 B-cell chronic lymphocytic leukemia by FISH

deletion 20q12 AML, MDS by FISH »

DiGeorge/Velo-Cardio-Facial syndrome deletion 22q11.2 by FISH

DNA ploidy; cell cycle analysis and S Phase by FLOW »

E

EGFR1 Epidermal growth factor receptor (HER1) by IHC »

EGFR/CEP7 (HER1/erb-B1) breast, lung and colon cancer by FISH

EGR1 -5/del 5q31 AML, MDS by FISH »

Estrogen/Progesterone receptors by IHC»

EWSR1 22q12 Ewing sarcoma by FISH

F

Factor II ( Prothrombin) G20210A mutation »

Factor V (Leiden) G1691A/R506Q mutation »

FIP1L1/PDGFRA (4q12) hypereosinophilia, mast cell by FISH

FLT3 mutation analysis acute myelogenous leukemia »

Friedreich Ataxia mutation gene sequencing »

Flow Cytometry

Comprehensive leukemia and/or lymphoma evaluation »

Targeted evaluation »

Lymphocyte screen »

Monoclonal gammopathy (B-cell/plasma cell) »

Myeloid screen »
Other markers »

Residual disease »

ZAP 70 »

G

Gleevec® resistance and ABL Kinase mutation »

H

HER2/neu PathVysion® breast cancer by FISH »
Herceptest by IHC »

Herpes Simplex virus Type 1 and Type 2 qualitative by real-time PCR
Hepatitis C virus genotype by Invader assay
Hepatitis C virus RNA qualitative by real-time PCR »

Hepatitis C virus RNA quantitative by real-time PCR »

Human identity genotyping, STR-PCR
Human Immunodeficiency virus quantitation by PCR
Human Immunodeficiency virus ultrasensitive quantitation by PCR
Human Immunodeficiency virus genotype
Human Immunodeficiency virus phenotype
Human papillomavirus genotyping
Human papillomavirus high risk by hybrid capture® II »

Hyperdiploidy 5, 9, 15 myeloma by FISH

I

IGH/CCND1 t(11;14) mantle cell lymphoma, (BCL1) by FISH »
IGH/BCL2 t(14;18) follicular cell lymphoma, (BCL2) by FISH »
IGH/FGFR3 t(4;14) myeloma by FISH
IGH 14q32 non Hodkin lymphoma, myeloma by FISH
IGH/MAF t(14;16) myeloma by FISH
IGH/MALT1 t(14;18) MALT lymphoma by FISH
IGH/MYC, CEP 8 t(8;14) Burkitt lymphoma by FISH
Immunohistochemistry markers available for:

Breast, colon, prostate, thyroid and other cancers
Dermatopathology
Hematoptopathology
Infectious agents
Neuropathology
Specialty:

Cytokeratins,

Endothelial,

Epithelial »

Mesothelioma,

Microsatellite instability,

ProExC™ biomarker »

J

JAK2 V617F mutation analysis Ph.neg. chronic myeloprolifertaive disorders »

K

Kallmann syndrome del KAL1(Xp22.3) by FISH
KRAS mutation and EGFR inhibitor response »

Ki67 by IHC »

L

Leukemia and/or lymphoma comprehensive evaluation by flow cytometry »
Leukocyte Adhesion deficiency (CD11a, CD11b, CD11c, CD18) by flow cytometry
Leukoreduced WBC count by FLOW »

Lymphocyte analysis(T-cell subsets, CD19, CD56) by flow cytometry  »

M

MALT118q21 MALT lymphoma by FISH

Maternal serum Alphafetoprotein

Maternal serum quad screen

MLL 11q23 AML by FISH »

Methylenetetrahydrofolate reductase mutation C677T and A1298C mutations »
Methylenetetrahydrofolate reductase mutation C677T mutation »

Miller-Dieker syndrome / Lissencephaly LIS1/RARA del

MYB deletion 6 chronic lymphocytic leukemia by FISH

Myelodysplasia profile includes:

EGR1 -5/ del 5q, CEP 7 -7/del 7q31, +8, del 20q12

Myeloma profile includes:

+5 / +9 / +15, del 13q14.3, p53 del 17p13.1, IGH 14q32

Myeloproliferative disorder profile includes:

BCR/ABL 9q34 t(9;22), +8, del 13q14.3, del 20q12

 

N

Neisseria gonorrhoeae qualitative by Aptima COMBO® 2 »

N-MYC 2p24.1 neuroblastoma by FISH

 

O

Olgodendroglioma del 1p36 / del 19q13 glioma by FISH

P

P53 del 17p13.1 various by FISH
Paroxysmal nocturnal hemoglobinuria (CD55, CD59) by flow cytometry »
Plasminogen Activator Inhibitor type 1 4G/5G polymorphism »

Phelan-McDermid syndrome N25/ARSA del 22q13.3 by FISH
PML-RARA t(15;17) acute promyelocytic leukemia by FISH »

PML-RARA t(15;17 short and long form quantitative by PCR »
Prader-Willi/Angelman del 15q11-q13 by FISH
ProEx™C biomarker by IHC »
PTEN/CEP10 del 10q23 by FISH

 

R

S

Smith-Magenis syndrome del 17p11.2 by FISH
SRY/CEP X del Yp11.3 by FISH
Steroid Sulfatase deficiency STS/CEP X for X-linked ichthyosis by FISH
SYT 18q11.2 synovial sarcoma by FISH
Subtelomeres, TelVysion by FISH

Surgical Pathology consultation

Surgical Pathology professional

T

T cell receptor gamma gene rearrangement by PCR »
T-cell subsets (CD3, CD4, CD8, CD4:CD8) by flow cytometry »
TEL/AML1 ES t(12;21) acute lymphoblastic leukemia by FISH
TelVysion: subtelomeres by FISH
trisomy 3 myeloma by FISH
trisomy 4 pediatric ALL by FISH
trisomy 6 ALL by FISH
trisomy 7 myeloma by FISH
trisomy 8 MDS, MPD by FISH »
trisomy 9 ALL, MDS, AML by FISH
trisomy 10 pediatric ALL
trisomy 12 CLL by FISH

U

UGT1A1 genotyping for Camptosar™ toxicity risk »
UroVysion®: +3 / +7 / +17 / del 9p21 bladder cancer by FISH

V

W

Warfarin Sensitivity, CYP2C9 and VKORC1 allele »
Williams syndrome del 7q11.23 by FISH
Wolf-Hirschhorn syndrome del 4p16.3 by FISH

XYZ

X/Y post sex-mismatch transplant by FISH

del Xp22.3 Kallmann syndrome by FISH

del Yp11.3 SRY/CEP X by FISH

ZAP 70 by flow cytometry »

123

1p36/del 19q13 glioma by FISH

2p23 ALK by FISH
2p24.1 N-MYC by FISH

trisomy 3 by FISH

3q27 BCL6 by FISH
+3/+7/+17/del 9p21 UroVysion® by FISH

trisomy 4 pediatric by FISH
del 4p16.3 Wolf-Hirschorn syndrome by FISH
(4q12) FIP1L1-PDGFRA by FISH
t(4;14) IGH/FGFR3 by FISH

del 5p15.2 Cri-du-Chat syndrome by FISH
+5/+9/+15 Hyperdiploidy by FISH
-5/del 5q31 EGR1 by FISH

del 6 MYB by FISH
trisomy 6 by FISH

trisomy 7 by FISH
del 7q11.23 Williams sndrome by FISH
-7/del 7q31 CEP 7 by FISH

trisomy 8 by FISH
8q24 CMYC by FISH
t(8;14) IGH/MYC, CEP 8 by FISH
t(8;21) AML1/ETO by FISH

trisomy 9 by FISH
del 9q34 ASS by FISH
9q34 t(9;22) BCR/ABL by FISH
(9;22) BCR/ABL p210 major quantitative by PCR
t(9;22) BCR/ABL minor p190 quantitative by PCR

del 10q23 PTEN/CEP10 by FISH
trisomy 10 by FISH

11q23 MLL by FISH
del 11q22.3 ATM by FISH
t(11;14) IGH/CCND1 (BCL1) by FISH
t(11;18) API2/MALT1 by FISH

trisomy 12 by FISH
t(12;21) TEL/AML1 ES by FISH

del 13q14.3 by FISH
+13/+18/+21/X/Y AneuVysion by FISH

14q32 IGH by FISH
t(14;16) IGH/MAF by FISH
t(14;18) IGH/BCL2 (BCL2) by FISH
t(14;18) BCL2 gene rearrangment by PCR
t(14;18) IGH/MALT1 by FISH

del 15q11q13 Prader-Willi / Angelman syndrome by FISH
t(15;17) PML/RARA by FISH
t(15;17) PML/RARA short and long form quantitative by PCR

t(16;16), inv(16) CBFB by FISH

del 17p11.2 Smith-Magenis syndrome by FISH
del 17p13.1 p53 by FISH
del 17p13.3 Miller-Dieker syndrome / Lissencephaly LIS1/RARA by FISH

18q11.2 SYT by FISH
18q21 MALT1 by FISH

del 20q12 by FISH

trisomy 21 by FISH

22q12 EWSR1 by FISH
del 22q13.3 Phelan-McDermid syndrome N25/ARSA by FISH
del 22q11.2 DiGeorge/Velo-Cardio-Facial syndrome by FISH