Results 321 to 330 of about 737,082 (371)

Clinical and Genetic Significance of Chromosomal Microarray Screening of Asymptomatic Newborns

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
Among 99 asymptomatic newborns with abnormal low‐resolution chromosomal microarray (LR‐CMA) screening, 70.7% harbored microduplication/microdeletions with syndromic implications. However, only a minority exhibited developmental concerns during early follow‐up, highlighting the need for cautious interpretation.
Naye Choi, Hwa Young Kim, Jung Min Ko
wiley   +1 more source

Feature Selection for Hypertension Risk Prediction Using XGBoost on Single Nucleotide Polymorphism Data. [PDF]

open access: yesHealthc Inform Res
Muflikhah L   +5 more
europepmc   +1 more source

Dual single‑nucleotide polymorphism biomarker combination for opioid selection to treat cancer pain. [PDF]

open access: yesMol Clin Oncol
Fujita Y   +16 more
europepmc   +1 more source

Applications and Challenges of Digital Health in Rheumatology

open access: yes
iNew Medicine, EarlyView.
Xiao‐Xiao Li   +4 more
wiley   +1 more source

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