Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG). Read more about Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG).
Primary care providers' responses to unsolicited Lynch syndrome secondary findings of varying clinical significance. Read more about Primary care providers' responses to unsolicited Lynch syndrome secondary findings of varying clinical significance.
The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant. Read more about The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant.
Reproductive outcomes in individuals with chromosomal reciprocal translocations. Read more about Reproductive outcomes in individuals with chromosomal reciprocal translocations.
Laboratory business models and practices: implications for availability and access to germline genetic testing. Read more about Laboratory business models and practices: implications for availability and access to germline genetic testing.
DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Genomics (ACMG). Read more about DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Genomics (ACMG).
DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG). Read more about DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG).
A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features. Read more about A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features.
Private payer coverage policies for ApoE-e4 genetic testing. Read more about Private payer coverage policies for ApoE-e4 genetic testing.
Evidence in the UK Biobank for the underdiagnosis of erythropoietic protoporphyria. Read more about Evidence in the UK Biobank for the underdiagnosis of erythropoietic protoporphyria.
