Raising Awareness and Education of Genetic Testing and Counseling through Fotonovelas among Latina Women At Risk for Hereditary Breast or Ovarian Cancer
“Living With a Question Mark”: Psychosocial Experience of Portuguese Young Adults at Risk for Hereditary Amyloid Transthyretin Amyloidosis With Polyneuropathy
Prevalence of Congenital Anomalies and Prenatal Diagnosis by Socioeconomic Level: Indicators of Inequality in Access to Elective Termination of Pregnancy for Fetal Anomalies
Research participant perceptions of personal utility in disclosure of individual research results from genomic analysis
Key Contextual Factors Involved with Participation in Medical and Genomic Screening and Research for African American and Caucasian Americans: A Qualitative Inquiry American Journal of Community Genetics
Psychosocial impacts on patients with Hypertrophic Cardiomyopathy (HCM) who received a Variant of Uncertain Significance (VUS) genetic test result
Comparative assessment of quality of life among adolescents with sickle cell disease and sickle cell trait: evidence from Odisha, India
The importance of geographic and sociodemographic aspects in the characterization of mucopolysaccharidoses: a case series from Ceará state (Northeast Brazil)
Caregiver-Reported Barriers to Care for Children and Adults with Williams Syndrome
Exploring family communication preferences in hereditary breast and ovarian cancer and Lynch syndrome: A national Canadian survey