Associated Papers
Analysis of X-inactivation status in a Rett syndrome natural history study cohort.
Fang X et al.
Molecular Genetics & Genomic Medicine, 2022
35318820 (PubMed )
Supplement: MGG3-10-e1917-s002.xlsx › Sheet1
MECP2 mutations in Serbian Rett syndrome patients.
Djarmati A et al.
Acta Neurologica Scandinavica, 2007
Select a paper to view details