共 50 条
- [32] Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females [J]. JOURNAL OF MOLECULAR MEDICINE-JMM, 2001, 78 (11): : 648 - +
- [35] MeCP2 mutations in children with and without the phenotype of Rett syndrome [J]. NEUROLOGY, 2001, 56 (11) : 1486 - 1495
- [38] Screening for mutations in exon 1 of MECP2, among individuals with either Rett syndrome, autism or mental retardation [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 130B (01): : 104 - 104
- [39] Characterization of large deletions of the MECP2 gene in Rett syndrome patients by gene dosage analysis [J]. MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (08):