A New Edition of European Journal of Human Genetics Is Now Available
May 24, 2021
European Journal of Human Genetics (vol. 28, no. 7, 2018) is available online by subscription only.
Articles include:
- “The Genetic History of France” by Aude Saint Pierre, et al.
- “Clinical Genomic Testing: What Matters to Key Stakeholders?” by Stephanie Best, et al.
- “Parents’ Motivations, Concerns and Understanding of Genome Sequencing: A Qualitative Interview Study” by Celine Lewis, et al.
- “Recommendations for Designing Genetic Test Reports to be Understood by Patients and Non-Specialists” by George D. Farmer, et al.
- “Development and Mixed-Methods Evaluation of an Online Animation for Young People about Genome Sequencing” by Celine Lewis, et al.
- “Relationships between Patient- and Session-Related Variables and Outcomes of Psychiatric Genetic Counseling” by Sarah Gerrard, et al.
- “Broad Consent in Practice: Lessons Learned from a Hospital-Based Biobank for Prospective Research on Genomic and Medical Data” by Gaia Barazzetti, et al.
- “The Genetic Architecture of Stargardt Macular Dystrophy (STGD1): A Longitudinal 40-Year Study in a Genetic Isolate” by Jane S. Green, et al.
- “Smith–Lemli–Opitz Syndrome: What is the Actual Risk for Couples Carriers of the DHCR7:c.964-1G>C Variant?” by Hagit Daum, et al.
- “Second Case of Bardet–Biedl Syndrome caused by Biallelic Variants in IFT74” by Lotte Kleinendorst, et al.
- “Cryptic Exon Activation causes Dystrophinopathy in two Chinese Families” by Ming Jin, et al.
- “Parental Repeat Length Instability in Myotonic Dystrophy Type 1 Pre- and Protomutations” by Isis B. T. Joosten, et al.
- “Alternate Approach to Stroke Phenotyping Identifies a Genetic Risk Locus for Small Vessel Stroke” by Joanna von Berg, et al.
