1 Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese pati..
来源:BMC MED GENET( P 1471-2350 E ) 发表时间: 2014/02
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2 Familial cases and male cases with MECP2 mutations
来源:AM J MED GENET B( P 1552-4841 E 1552-485X ) 发表时间: 2017/06
类型:期刊论文 为本人加分:358.975508
3 MECP2 duplication syndrome in a Chinese family
来源:BMC MED GENET( P 1471-2350 E ) 发表时间: 2015/12
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4 Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort
来源:GENET MED( P 1098-3600 E 1530-0366 ) 发表时间: 2019/06
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5 Molecular characteristics of Chinese patients with Rett syndrome
来源:EUR J MED GENET( P 1769-7212 E 1878-0849 ) 发表时间: 2012/12
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6 Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
来源:BMC MED GENET( P 1471-2350 E ) 发表时间: 2017/08
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7 Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort[vol 21, pg 1330, 201..
来源:GENET MED( P 1098-3600 E 1530-0366 ) 发表时间: 2019/09
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