Increasing demand and workforce shortages impact access to genetic services

Measuring the cost of genetic disorders in hospitalized children

Prenatal and preimplantation genetic diagnosis for Huntington disease in the UK

New approaches help to further unravel the genetic etiologies of autism

Improved diagnostic yield from exome sequencing following re-evaluation by clinical geneticists

Somatic mosaicism for genetic variants in brain tissue @emdash; a contributor to neurogenetic disease?

Dealing with misattributed parentage in the clinical genetics laboratory

Newborn Screening Bringing good data to bear remains critical

Changing Interpretations of Sequencing Results - Clinical Impact in the Realm of Hereditary Cancers

Shedding light on intragenic deletions and duplications

High numbers of false positive results in Direct To Consumer testing samples

Drinking the Kool-Aid? How the popular press has portrayed personalized medicine

Lab reports of genetic tests...lots of room for improvement

CLAPO Syndrome, PIK3CA and lessons for how to categorize genetic disease

Keeping Science from getting lost in translation

Beyond 21, 18 and 13: Broadening applications of Non Invasive Prenatal Screening

New Estimates of the Penetrance of Hemochromatosis: Time to re-think screening?

Diversity in Genomics...Necessary for All of Us

Moving therapeutics ahead in Genomics: response to imatinib in infantile myofibromatosis

Extending Whole Exome Sequencing to the prenatal period