A New Edition of Genetics in Medicine Is Now Available

October 5, 2021

Genetics in Medicine (vol. 23, no. 4, 2021) is available online by subscription only.

Articles include:

• “Evaluating the Resource Implications of Different Service Delivery Models for Offering Additional Genomic Findings” by Martin Vu, et al.
• “Private Payer Coverage Policies for ApoE-e4 Genetic Testing” by Jalayne J. Arias, et al.
• “De Novo Variants in MED12 cause X-linked Syndromic Neurodevelopmental Disorders in 18 Females” by D. L. Polla, et al.
• “Biallelic UBE4A Loss-of-Function Variants cause Intellectual Disability and Global Developmental Delay” by Uirá Souto Melo, et al.
• “CNV Profiles of Chinese Pediatric Patients with Developmental Disorders” by Haiming Yuan, et al.
• “Risk-Reducing Hysterectomy and Bilateral Salpingo-Oophorectomy in Female Heterozygotes of Pathogenic Mismatch Repair Variants: A Prospective Lynch Syndrome Database Report” by Mev Dominguez-Valentin, et al.
• “Health and Economic Outcomes of Newborn Screening for Infantile-Onset Pompe Disease” by John S. Richardson, et al.
• “Methods and Feasibility Study for Exome Sequencing as a Universal Second-Tier Test in Newborn Screening” by Nicole Ruiz-Schultz, et al.