Identification of mutation carriers and referral to genetic services

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Outcomes

More accurate diagnosis and risk assessment of family members

Screening and surveillance for mutation carriers and family members

Identification of mutation carriers in the family

Identification and referral to genetic services

Reinforcing factors

Referral process

Patient request

Clinical guidelines

History

Personal

Family

Enabling factors

Access to and availability of genetic services

Cost

Wait time

Predisposing factors

Clinician demographics

Awareness

Knowledge

Confidence