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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: 15q24 Microdeletion Syndrome[original query]
Genomic Analyses of Patients With Unexplained Early-Onset Scoliosis.
Spine deformity 2014 (5): 324-332.
Gao Xiaochong, Gotway Garrett, Rathjen Karl, Johnston Charles, Sparagana Steven, Wise Carol
Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China.
Pediatrics and neonatology 2018 Mar .
Wang Rongyue, Lei Tingying, Fu Fang, Li Ru, Jing Xiangyi, Yang Xin, Liu Juan, Li Dongzhi, Liao C
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