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- ACMG
Discover the latest in genetic healthcare with the ACMG Education Webinar Series: Translating Genes into Health® Specialized events developed by ACMG Committees Learn More
- Practice Guidelines - ACMG
Noninvasive prenatal screening for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG) (includes Correction)
- ACT Sheets and Algorithms - ACMG
The ACMG ACT Sheets and their accompanying algorithms are a great resources for health care providers looking for information on genetic conditions (identified through newborn screening and beyond) to help inform clinical decision making
- Education and Events - ACMG
Advance YOUR genetics and genomics career through educational programs offered by the ACMG From the fundamentals of genetics and genomics to the best practices of clinical care, participate in the learning opportunities ACMG offers to physicians, scientists and health professionals
- Technical Standards and Guidelines - acmg. net
The Find Genetic Services Directory is provided as a general resource for physicians and others seeking medical genetic services ACMG does not endorse or warrant the quality of the services provided by these individuals or their institutions
- Meetings and Events - ACMG
The ACMG sponsors an Annual Clinical Genetics Meeting and other events offering educational content in clinical genetics with the purpose of serving its members, other healthcare professionals and the public
- American College of Medical Genetics and Genomics (ACMG), ACMG . . .
American College of Medical Genetics and Genomics (ACMG) - Find your next career at ACMG Employment Resource Center Check back frequently as new jobs are posted every day
- Standards and guidelines for the interpretation of sequence . . . - ACMG
ACMG StAndArdS And GuidelineS Interpretation of sequence variants INTRODUCTION Clinical molecular laboratories are increasingly detecting novel sequence variants in the course of testing patient specimens for a rapidly increasing number of genes associated with genetic disorders While some phenotypes are associated with a single
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