Mei Peng

The direction of microsatellite mutations is dependent upon allele length

Xin Xu, Mei Peng, Zhian Fang et al. · Nature Genetics · 2000 · 371 citations

Genetic Analysis, Allelic Variant, Linkage Disequilibrium +8

Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: Implications for fragile X syndrome carrier and newborn screening

Feras Hantash, Dana G. Goos, David Tsao et al. · Genetics in Medicine · 2010 · 83 citations · Full text

Genetic Testing, Mendelian Disorder, Genetic Disorder +12

Molecular testing for Fragile X Syndrome: Lessons learned from 119,232 tests performed in a clinical laboratory

Charles M. Strom, Beryl Crossley, Joy B. Redman et al. · Genetics in Medicine · 2007 · 62 citations · Full text

Fragile X Syndrome, Genetic Testing, Mendelian Disorder +12

Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivation

Lauren S Marshall, Julie Simon, Tim Wood et al. · BMC Medical Genetics · 2013 · 48 citations · Full text

Black phosphorus thermosensitive hydrogels loaded with bone marrow mesenchymal stem cell-derived exosomes synergistically promote bone tissue defect repair

Yongmei Hua, Mei Peng, Deliang Zeng et al. · Journal of Materials Chemistry B · 2023 · 42 citations