Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1
S Datta, MP Alam, SS Majumdar, AK Mehta… - Chromosome …, 2011 - Springer
The expansion of CGG repeats in the 5′-untranslated region (5′ UTR) of FMR1 gene is
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1
S Datta, MP Alam, SS Majumdar, AK Mehta… - Chromosome …, 2011 - repository.ias.ac.in
The expansion of CGG repeats in the 5′-untranslated region (5′ UTR) of FMR1 gene is
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1
S Datta, MP Alam, SS Majumdar… - … journal on the …, 2011 - pubmed.ncbi.nlm.nih.gov
The expansion of CGG repeats in the 5'-untranslated region (5'UTR) of FMR1 gene is the
molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
[引用][C] Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1
S Datta, MP Alam, SS Majumdar, AK Mehta… - Chromosome …, 2011 - cir.nii.ac.jp
Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet
repeat region from mouse and human fragile X mental retardation gene 1 | CiNii Research …
repeat region from mouse and human fragile X mental retardation gene 1 | CiNii Research …
[PDF][PDF] Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene
S Datta, MP Alam, SS Majumdar, AK Mehta… - Chromosome …, 2011 - researchgate.net
The expansion of CGG repeats in the 5′-untranslated region (5′ UTR) of FMR1 gene is
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1.
S Datta, M Alam, S Majumdar, A Mehta… - Chromosome …, 2011 - search.ebscohost.com
The expansion of CGG repeats in the 5′-untranslated region (5′ UTR) of FMR1 gene is
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1.
S Datta, MP Alam, SS Majumdar, AK Mehta… - … Journal on the …, 2011 - europepmc.org
The expansion of CGG repeats in the 5'-untranslated region (5'UTR) of FMR1 gene is the
molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1
S Datta, MP Alam, SS Majumdar… - Chromosome …, 2011 - search.proquest.com
The expansion of CGG repeats in the 5'-untranslated region (5'UTR) of FMR1 gene is the
molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1
S Datta, MP Alam, SS Majumdar, AK Mehta… - Chromosome …, 2011 - infona.pl
The expansion of CGG repeats in the 5′-untranslated region (5′ UTR) of FMR1 gene is
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1
S Datta, MP Alam, SS Majumdar, AK Mehta… - Chromosome …, 2011 - repository.ias.ac.in
The expansion of CGG repeats in the 5′-untranslated region (5′ UTR) of FMR1 gene is
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …
the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking …