Medical Education

We understand, no matter what field of medicine you practice, it is important to keep up with the most recent medical trends and information. That is why we established our National Speakers Bureau.

Our National Speakers Bureau is a group of medical thought leaders that includes M.D. and Ph.D. geneticists, who are certified by the American Board of Medical Genetics, and genetic counselors. The members of the bureau are available to make presentations or give lectures on the latest medical trends in genetics.

The National Speakers Bureau is an excellent resource for grand rounds, medical and managed care symposia, in-services, residency training programs and other medical education forums.

Over 50 lectures are available in the following subject areas:

• Human genetics
• Prenatal diagnosis
• Cancer genetics
• DNA diagnostic/single gene disorders
• Topical issues, such as ethical and legal considerations in genetic testing and pre-dispositional testing

Lectures range in degree from introductory to advanced difficulty. Average lectures run one hour. Multiple lectures can be combined for half- or full-day programs.

The National Speakers Bureau content is appropriate for a variety of clinical disciplines:

• Primary care physicians
• Geneticists and genetic counselors
• Medical specialists in: maternal fetal medicine, obstetrics, hematology, oncology, neurology, pediatrics and pathology
• Laboratory professionals
• Nursing professionals
• Case management professionals

We also have an array of educational brochures that outline the various types of reproductive tests we offer. If you would like to review any of these pieces, visit the Overview of Services section of our site and download a PDF. You can also call our Client Services Department at (800) 848-4436 and request copies of a brochure.

		Search by Test Name or Condition:
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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