Pallabi De

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  • R De Franchis, A Buoninconti, +63 authors Jasonni V Currarino
  • 2011
The C677T mutation of the 5,10-methylentetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy. A genetic polymorphism in the human HOXB1 homeobox gene implying a 9bp tandem repeat in the amino-terminal coding region. Mutations in brief #200. Spinal Dysgenesis: neuroradiologic findings with clinical and embryologic correlation.(More)
BACKGROUND Functional immunoglobulin and T cell receptor genes are produced in developing lymphocytes by V(D)J recombination. The initial site-specific DNA cleavage steps in this process are catalyzed by the V(D)J recombinase, consisting of RAG1 and RAG2, which is directed to appropriate DNA cleavage sites by recognition of the conserved recombination(More)
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