Hasil Pencarian - Subba Rao Indugula

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  1. 1
    Exome sequencing identified a novel HIST1H1E heterozygous protein‐truncating variant in a 6‐month‐old male patient with Rahman syndrome: A case report

    Exome sequencing identified a novel HIST1H1E heterozygous protein‐truncating variant in a 6‐month‐old male patient with Rahman syndrome: A case report oleh Subba Rao Indugula, Sofia Saenz Ayala, Francesco Vetrini, Alyce Belonis, Wenying Zhang

    Diterbitkan 2022-02-01
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  2. 2
    A genome-wide linkage scan identifies multiple chromosomal regions influencing serum lipid levels in the population on the Samoan islands*s⃞

    A genome-wide linkage scan identifies multiple chromosomal regions influencing serum lipid levels in the population on the Samoan islands*s⃞ oleh Karolina Åberg, Feng Dai, Guangyun Sun, Ember Keighley, Subba Rao Indugula, Linda Bausserman, Satupaitea Viali, John Tuitele, Ranjan Deka, Daniel E. Weeks, Stephen T. McGarvey

    Diterbitkan 2008-10-01
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  3. 3
    Finding missing heritability in less significant Loci and allelic heterogeneity: genetic variation in human height.

    Finding missing heritability in less significant Loci and allelic heterogeneity: genetic variation in human height. oleh Ge Zhang, Rebekah Karns, Guangyun Sun, Subba Rao Indugula, Hong Cheng, Dubravka Havas-Augustin, Natalija Novokmet, Zijad Durakovic, Sasa Missoni, Ranajit Chakraborty, Pavao Rudan, Ranjan Deka

    Diterbitkan 2012-01-01
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  4. 4
    Extent of height variability explained by known height-associated genetic variants in an isolated population of the Adriatic coast of Croatia.

    Extent of height variability explained by known height-associated genetic variants in an isolated population of the Adriatic coast of Croatia. oleh Ge Zhang, Rebekah Karns, Guangyun Sun, Subba Rao Indugula, Hong Cheng, Dubravka Havas-Augustin, Natalija Novokmet, Dusko Rudan, Zijad Durakovic, Sasa Missoni, Ranajit Chakraborty, Pavao Rudan, Ranjan Deka

    Diterbitkan 2011-01-01
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  5. 5
    Clinical impact and cost-effectiveness of whole exome sequencing as a diagnostic tool: a pediatric center’s experience

    Clinical impact and cost-effectiveness of whole exome sequencing as a diagnostic tool: a pediatric center’s experience oleh C. Alexander Valencia, Ammar eHusami, Jennifer eHolle, Judith A. Johnson, Yaping eQian, Abhinav eMathur, Chao eWei, Subba Rao Indugula, Fanggeng eZou, Haiying eMeng, Lijun eWang, Xia eLi, Rachel eFisher, Tony eTan, Amber eHogart Begtrup, Kathleen eCollins, Katie A. Wusik, Derek eNeilson, Thomas eBurrow, Elizabeth eSchorry, Robert eHopkin, Mehdi eKeddache, John Barker Harley, Kenneth M. Kaufman, Kejian eZhang

    Diterbitkan 2015-08-01
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