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[DOI] [PubMed] [Google Scholar] 77.Alizadeh M., Karimi F., Fallah M.R
By: R on2024-07-30 16:44:15
Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband
After in situ mRNA hybridization of extruded germlines, both mpk-1ab and mpk-1b specific probes were low in the mitotic region, increased in the transition zone, and became abundant in the pachytene and oogenic regions (Figure 1D and 1E)
doi:10.1101/cshperspect.a026633
