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Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry
The association between frailty and MRI features of cerebral small vessel disease
The association between frailty and MRI features of cerebral small vessel disease
Cerebral microbleeds are not associated with postoperative delirium and postoperative cognitive dysfunction in older individuals
SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy
CACNA1B mutation is linked to unique myoclonus-dystonia syndrome
Homozygous and Compound-Heterozygous Mutations in TGDS Cause Catel-Manzke Syndrome
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling