Results 181 to 190 of about 2,018 (241)

Three novel heterozygous ANK1 loss-of-function variants cause hereditary spherocytosis in Chinese families. [PDF]

open access: yesAnn Hematol
Wang Y   +8 more
europepmc   +1 more source

ANK3 as a Novel Genetic Biomarker for Liafensine in Treatment-Resistant Depression: The ENLIGHTEN Randomized Clinical Trial. [PDF]

open access: yesJAMA Psychiatry
Wang G   +14 more
europepmc   +1 more source

Plenary Abstracts Session & Oral Presentations

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Publication Only

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Home - About - Disclaimer - Privacy