General Specimen Requirements

• Label all tubes
• Close all tubes and canisters tightly
• Enclose completed paperwork

For more detailed specimen requirement information, review our Quick Reference Guide.

Shipping Information / Supply Order Form

• In hot weather, enclose refrigerated (not frozen) gel pack in Styrofoam box
• In cold weather, run hot water over gel pack for 3-5 minutes and enclose
• Ship specimens within 24 hours via Federal Express, Priority and Saturday delivery
• Call or fax Genzyme Genetics Client Services regarding the receiving laboratory and air bill tracking number

Use our Supply Order Form to get the materials you need.

Location	Call for Local Pick-Ups	Fax Number
Los Angeles, CA 5300 McConnell Avenue Los Angeles, CA 90066	(800) 447-5816	(310) 482-5001
Monrovia, CA 655 East Huntington Drive Monrovia, CA 91016	(800) 255-1616	(626) 471-7510
New York, NY 521 West 57th Street Sixth Floor New York, NY 10019	(800) 447-8881	(212) 258-2137
Orange, CA 1054 Town & Country Road Orange, CA 92868-4714	(800) 745-4363	(714) 245-9259
Phoenix, AZ 810 East Hammond Lane Phoenix, AZ 85034	(800) 645-6626	(602) 254-7340
Santa Fe, NM 2000 Vivigen Way Santa Fe, NM 87505	(800) 848-4436	(505) 438-2270
Tampa, FL 10421 University Center Drive Suite 100 Tampa, FL 33612	(800) 966-4440	(813) 972-4632
Westborough, MA 3400 Computer Drive Westborough, MA 01581	(800) 255-7357	(508) 389-5549

Feel free to review our shipping kits certification documents:

Canisters
Formalin containers
2-Pak shippers
4-Pak shippers

If you are unsure where to send a particular specimen, please call our Client Services Department at (800) 848-4436.

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		Select a test .... Acetylcholinesterase (AChE) Testing AFP3® - Triple Marker Test AFP4® - Quadruple Marker Test Amniotic Fluid Alphafetoprotein (AFAFP) Testing Angelman Syndrome Protocol Angiotensin Converting Enzyme (ACE) Analysis Ashkenazi Jewish Carrier Testing Bloom Syndrome Mutation Analysis Canavan Disease Mutation Analysis CFTR Intron 8 Poly (T) Analysis Chitotriosidase Assay Cri-Du-Chat Microdeletion Analysis Cystic Fibrosis Expanded Mutation Analysis - CFplus™ Cystic Fibrosis Gene Sequencing Cytogenetics – Amniotic Fluid Chormosome Analysis Cytogenetics – Blood Chromosome Analysis Cytogenetics – Chorionic Villi Sampling Chromosome Analysis Cytogenetics – Chromosome Breakage Analysis (Blood) Cytogenetics – Products of Conception (POC) Chromosome Analysis DiGeorge/Velocardiofacial (22q11) Syndrome Microdeletion Analysis Fabry Disease Enzyme Analysis Fabry Disease Mutation Analysis by Sequencing Factor II (Prothrombin) G20210A Mutation Analysis Factor V Leiden Mutation Analysis Familial Dysautonomia Mutation Analysis Fanconi Anemia Group C Mutation Analysis FirstScreen™ - First Trimester Screening Fragile X Syndrome Mutation Analysis Gaucher Disease Enzyme Analysis Gaucher Disease Mutation Analysis Glycogen Storage Disease Type 1a Mutation Analysis InSight (Interphase FISH for Rapid Detection of X, Y, 13, 18, 21) IntegratedScreen™ - Integrated Screening Kallmann Syndrome Microdeletion Analysis Maple Syrup Urine Disease (MSUD) Mutation Analysis Maternal Cell Contamination Analysis Maternal Serum Alphafetoprotein (MSAFP) Screening Microdeletion Analyses Miller-Dieker Syndrome Microdeletion Analysis MTHFR (C677T) Mutation Analysis Mucolipidosis Type IV Mutation Analysis Niemann-Pick Disease Type A Mutation Analysis Pompe Disease Test Pompe Disease Mutation Analysis (GAA) by Sequencing Prader-Willi Protocol Preimplantation Genetic Diagnosis (PGD) - Aneuploidy Preimplantation Genetic Diagnosis (PGD) - Translocations Rh c/E Mutation Analysis Rh D Mutation Analysis SequentialScreen™ SerumIntegratedScreen™ - Integrated Screening Sickle Cell Anemia Mutation Analysis Smith-Magenis Syndrome Microdeletion Analysis Spinal Muscular Atrophy (SMA) Steroid Sulfatase Deficiency (X-linked Ichthyosis) Subtelomere Analysis Tay-Sachs Disease Mutation Analysis Tay-Sachs Enzyme Analysis (Hexosaminidase A) TRAP (Tartrate Resistant Acid Phosphatase) Williams Syndrome Microdeletion Analysis Wolf-Hirschhorn Syndrome Microdeletion Analysis Y Chromosome Microdeletion Analysis Zygosity Testing