A New Edition of European Journal of Human Genetics Is Now Available

May 21, 2021

European Journal of Human Genetics (vol. 28, no. 6, 2018) is available online by subscription only.

Articles include:

  • “Exploring Broad Consent in the Context of the 100,000 Genomes Project: A Mixed Methods Study” by Lisa M. Ballard, et al.
  • “Unraveling the Genetic Cause of Hereditary Ophthalmic Disorders in Arab Societies from Israel and the Palestinian Authority” by Anja K. Mayer, et al.
  • “Identification of RELN Variant p.(Ser2486Gly) in an Iranian Family with Ankylosing Spondylitis; The first Association of RELN and AS” by Masoud Garshasbi, et al.
  • “De Novo Variants in CAMTA1 cause a Syndrome Variably Associated with Spasticity, Ataxia, and Intellectual Disability” by Iris G. M. Wijnen, et al.
  • “High-Resolution Inference of Genetic Relationships among Jewish Populations” by Naama M. Kopelman, et al.
  • “TCTEX1D1 is a Genetic Modifier of Disease Progression in Duchenne Muscular Dystrophy” by Pietro Spitali, et al.
  • “Transcript Specific Regulation of Expression Influences Susceptibility to Multiple Sclerosis” by Maria Ban, et al.

 

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Posted in Clinical / Medical, Disability Ethics, Education, Genetic Ethics, Global Bioethics, Healthcare, Human Dignity, Informed Consent, Journal Articles, Mental Health, Neuroethics, Public Health, Public Policy, Research Ethics

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