to a genetic clinic Children with congenital abnormalities (birth defects), learning disability, dysmorphic features Children with chromosomal disorders or inherited conditions Adults affected by congenital abnormality or an inherited condition Adults known to carry or at risk of carrying, a balanced chromosomal rearrangement Common reasons for referral to a genetic clinic Couples who have lost a child or stillborn baby with a congenital abnormality or inherited condition Couples who have suffered reproductive loss (termination of pregnancy for fetal abnormality or recurrent miscarriage) Couples who may transmit a genetic condition to their children Common reasons for referral to a genetic clinic Pregnant women and their partners, when fetal abnormality is detected Children and adults with a family history of a known genetic disorder Adults at risk of developing an inherited condition who may request predictive testing Individuals with a family history of a common condition with a strong genetic component, including familial cancers