Showing 1 - 4 results of 4 for search 'N Swapna', query time: 0.02s Refine Results
  1. 1
    PMM2-CDG T237M Mutation in a Patient with Cerebral Palsy-Like Phenotypes Reported from South India

    PMM2-CDG T237M Mutation in a Patient with Cerebral Palsy-Like Phenotypes Reported from South India by N. Sreedevi, N. Swapna, Santosh Maruthy, H.S. Meghavathi, Charles Sylvester

    Published 2023-06-01
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  2. 2
    Association of apolipoprotein ε4 allele with intellectual disability in children with cerebral palsy

    Association of apolipoprotein ε4 allele with intellectual disability in children with cerebral palsy by N Sreedevi, N Swapna, Santosh Maruthy, Rajesh Kundapur, Charles Sylvester

    Published 2023-01-01
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  3. 3
    Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive [version 1; referees: 2 approved]

    Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive [version 1; referees: 2 approve... by Desaraju Suresh Bhargav, N. Sreedevi, N. Swapna, Soumya Vivek, Srinivas Kovvali

    Published 2017-12-01
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  4. 4
    Marker-Assisted Backcrossing to Introgress Resistance to Fusarium Wilt Race 1 and Ascochyta Blight in C 214, an Elite Cultivar of Chickpea

    Marker-Assisted Backcrossing to Introgress Resistance to Fusarium Wilt Race 1 and Ascochyta Blight in C 214, an Elite Cultivar of Chickpea by R. K. Varshney, S. M. Mohan, P. M. Gaur, S. K. Chamarthi, V. K. Singh, S. Srinivasan, N. Swapna, M. Sharma, S. Pande, R. K. Varshney, S. Singh, L. Kaur

    Published 2014-03-01
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