遗传遗传学：当前研究

案例报告

Phenotypic Variability in Fraternal Twins with PEX1 Mutations: Zellweger Syndrome with Discordant Clinical Phenotype

• Janet Simons and Malgorzata JM Nowaczyk

评论文章

Genetic Complexity of Human Myelomeningocele

• Kit Sing Au and Hope Northrup

社论

Pleiotropy of Presenilins

• Airong Li

研究文章

High Expression Of Atp7b MRNA In The Peripheral Blood Mononuclear Cells Of The Long-Evans Cinnamon Rats: An Animal Model Of Wilsons Disease

• Kenji Nakayama1, Yoshinobu Katoh, Norikazu Shimizu, Toyo Okui, Kozo Matsumoto, Yukiharu Sawada, Tsugutoshi Aoki