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R

Rosaline C. M. Quinlivan

University of Pennsylvania
H指数:51
被引数:1.0万

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Liver function in X-linked myotubular myopathy and autosomal dominant centronuclear myopathy: Data of the unite-CNM study

X-连锁肌管性肌病和常染色体显性中间核肌病中的肝功能:unite-CNM研究的数据

2025-04-240
PRE
Long-term Natural History of Pediatric Dominant and Recessive RYR1-Related Myopathy
2023-10-102
PRE
Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencing

专家多学科投入通过全基因组测序最大化罕见疾病诊断

2022-11-0710
OAAI
Adult North Star Network (ANSN): Consensus Document for Therapists Working with Adults with Duchenne Muscular Dystrophy (DMD) - Therapy Guidelines
2022-02-043
OA
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis
BRAIN
IF11.7
2021-12-249
OA
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report

医疗保健中罕见疾病诊断的100,000基因组试点-初步报告

2021-11-11364
OAAI
Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study
2021-11-0341
OAAI
Expanding the molecular and phenotypic spectrum of truncating MT-ATP6 mutations
2020-02-0123
OAAI