Please be on the look out for
Ambry representatives at
The Clinical Genome Conference
San Francisco, CA
6/25 - 6/28
Ambry representatives at
The Clinical Genome Conference
San Francisco, CA
6/25 - 6/28
Clinical Resources
Ambry Genetics supports ongoing clinician education and sharing of data to help promote scientific discoveries that help improve patient management and care.
With that in mind, Ambry is excited to share several medians of educational materials with our colleagues.
Scientific Posters
- List of 2013 ACMG Abstracts
- Cancer Panel Data, Presented in NSGC, Boston 2012
- ColoNext NGS Panel Positive Findings
- ASCO Quality Care Symposium, 2012: Clinical Adoption of NGS for Hereditary Cancer
- Exome Sequencing Reveals a de novo DYNC1H1 Mutation
- Exome Sequencing Leads to a Timothy Syndrome Diagnosis
- Exome Sequencing Reveals a Novel C20orf7 Mutation
- Patient Decisions for Disclosure of Exome Sequencing Findings
- Beyond BRCA1/2, Genetic Testing for Hereditary Breast Cancer
- BreastNext Uptake and Usability in Clinical Practice
- APC Promotoer 1B Deletions in Association with FAP
- A novel HUWE1 missense mutation in a patient with intellectual disability
- A novel OPHN1 splice site mutation in a patient with mental retardation
- A novel intragenic deletion in SLC9A6 in a patient with intellectual disability
- A retrospective Genetic Analysis of Cases Reported using an XLMR/XLID Next-Generation Sequencing Panel
Webinars
- Autism Spectrum Disorders and the Genetic Link
Date: Wednesday, September 12, 2012 -
New Technologies and Your Practice: Understanding
Next-Gen Sequencing
Date: Tuesday, June 26, 2012
Webinar Slides
Scientific Presentations
- Bringing Clarity to Undiagnosed Neurologic Disease
- Clinical Diagnostic Exome: What have we found so far?
Clinician Brochures
- BreastNext
- ColoNext
- OvaNext
- Exome Sequencing
- Autism Spectrum Disorders
- XLID
- Hereditary Arrhythmia
- Hereditary Cardiovascular Testing
Patient Brochures
Other Publications