Search Results - Askree, S Hussain

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  1. 1
    Identification of an intronic Alu insertion in the SYNE1 gene associated with autosomal recessive spinocerebellar ataxia type 8

    Identification of an intronic Alu insertion in the SYNE1 gene associated with autosomal recessive spinocerebellar ataxia type 8 by Gagnon, Maryse, Bouhamdani, Nadia, Kolev, Dimiter P., Askree, S. Hussain, Ben Amor, Mouna

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  2. 2
    P751: Challenges in interpretation of RNA-Seq data limit variant reclassification

    P751: Challenges in interpretation of RNA-Seq data limit variant reclassification by Askree, S. Hussain, Reott, Michael, Stovall, Kirk, Kolev, Dimiter, Langley, William

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  3. 3
    Detection limit of intragenic deletions with targeted array comparative genomic hybridization

    Detection limit of intragenic deletions with targeted array comparative genomic hybridization by Askree, S Hussain, Chin, Ephrem L H, Bean, Lora H, Coffee, Bradford, Tanner, Alice, Hegde, Madhuri

    Published in BMC genetics
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  4. 4
    Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients

    Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients by Nallamilli, Babi Ramesh Reddy, Chakravorty, Samya, Kesari, Akanchha, Tanner, Alice, Ankala, Arunkanth, Schneider, Thomas, da Silva, Cristina, Beadling, Randall, Alexander, John J., Askree, Syed Hussain, Whitt, Zachary, Bean, Lora, Collins, Christin, Khadilkar, Satish, Gaitonde, Pradnya, Dastur, Rashna, Wicklund, Matthew, Mozaffar, Tahseen, Harms, Matthew, Rufibach, Laura, Mittal, Plavi, Hegde, Madhuri

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  5. 5
    P479: Mosaicism for genome wide homozygosity identified as an incidental finding in two healthy pregnant women

    P479: Mosaicism for genome wide homozygosity identified as an incidental finding in two healthy pregnant women by Haskell, Gloria, Askree, Hussain, Kline, Laura, Cabral, Quoc-Huong, Hasadri, Linda, Gadi, Inder, Schwartz, Stuart

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