Maternal cell-free DNA-based screening for fetal microdeletion and the importance of careful diagnostic follow-up. Read more about Maternal cell-free DNA-based screening for fetal microdeletion and the importance of careful diagnostic follow-up.
Reporting genomic secondary findings: ACMG members weigh in. Read more about Reporting genomic secondary findings: ACMG members weigh in.
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway. Read more about Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway.
Delivery of clinical genetic consultative services in the Veterans Health Administration. Read more about Delivery of clinical genetic consultative services in the Veterans Health Administration.
The economic value of personalized medicine tests: what we know and what we need to know. Read more about The economic value of personalized medicine tests: what we know and what we need to know.
Stakeholder engagement: a key component of integrating genomic information into electronic health records. Read more about Stakeholder engagement: a key component of integrating genomic information into electronic health records.
Ethical, legal, and social implications of incorporating genomic information into electronic health records. Read more about Ethical, legal, and social implications of incorporating genomic information into electronic health records.
Factors influencing organizational adoption and implementation of clinical genetic services. Read more about Factors influencing organizational adoption and implementation of clinical genetic services.
A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians. Read more about A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians.
Effective communication of molecular genetic test results to primary care providers. Read more about Effective communication of molecular genetic test results to primary care providers.
