Showing 1 - 6 results of 6 for search 'Rizwan Hamid', query time: 0.02s Refine Results
  1. 1
    Ambulatory Urodynamic Findings Change Patient Outcomes

    Ambulatory Urodynamic Findings Change Patient Outcomes by Richard G. Axell, Vahit Guzelburc, Habiba Yasmin, Bogdan Toia, Mahreen H. Pakzad, Rizwan Hamid, Jeremy L. Ockrim, Tamsin J. Greenwell

    Published 2021-11-01
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  2. 2
    RNA‐Seq and ChIP‐Seq Identification of Unique and Overlapping Target Genes and Pathways Regulated by TBX4 in Human Pulmonary Fibroblasts and Pericytes

    RNA‐Seq and ChIP‐Seq Identification of Unique and Overlapping Target Genes and Pathways Regulated by TBX4 in Human Pulmonary Fibroblasts and Pericytes by Ying Cai, Ling Yan, Joy D. Cogan, Lora K. Hedges, Bethany Nunley, Nick Negretti, Jennifer M. S. Sucre, James West, Eric D. Austin, Rizwan Hamid

    Published 2025-01-01
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  3. 3
    O31: X-linked inheritance results in different sex-specific phenotypes, penetrance, disease course, diagnostic odysseys, and newborn screening sensitivity in Fabry disease

    O31: X-linked inheritance results in different sex-specific phenotypes, penetrance, disease course, diagnostic odysseys, and newborn screening sensitivity in Fabry disease by Yutaka Furuta, Natalie Owen, Lisa Bastarache, Chelsea Lauderdale, Laila AI-Shaar, Elvira Ponce, Neena Agrawal, Camille Carter, Karee Morgan, Rizwan Hamid, John Phillips, Rory Tinker

    Published 2025-01-01
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  4. 4
    Fine mapping and identification of CaTTG1, a candidate gene that regulates the hypocotyl anthocyanin accumulation in Capsicum annuum

    Fine mapping and identification of CaTTG1, a candidate gene that regulates the hypocotyl anthocyanin accumulation in Capsicum annuum by Jin Wang, Yao Dai, Luzhao Pan, Ying Chen, Li Dai, Yanqing Ma, Xiaoxun Zhou, Wu Miao, Muhammad Rizwan Hamid, Xuexiao Zou, Feng Liu, Cheng Xiong

    Published 2025-01-01
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  5. 5
    Review and metabolomic profiling of unsolved case reveals newly reported autosomal dominant congenital disorder of glycosylation, type Iw formerly thought to only be an autosomal recessive condition

    Review and metabolomic profiling of unsolved case reveals newly reported autosomal dominant congenital disorder of glycosylation, type Iw formerly thought to only be an autosomal r... by Kimberly M. Ezell, Yutaka Furuta, Devin Oglesbee, Eniko K. Pivnick, David Rinker, Jonathan H. Sheehan, Rory J. Tinker, Rizwan Hamid, Joy D. Cogan, Lynette Rives, Serena Neumann, Brian Corner, Mary Koziura, John A. Phillips, III

    Published 2024-12-01
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  6. 6
    P460: Case series of Nizon-Isidor syndrome by heterozygous variants in MED12L with one case generating chromosomal instability through diploid-triploid mosaicism

    P460: Case series of Nizon-Isidor syndrome by heterozygous variants in MED12L with one case generating chromosomal instability through diploid-triploid mosaicism by Russell Stewart, Kimberly Ezell, Brian Corner, Ashley McMinn, Joy Cogan, Rizwan Hamid, Lynette Rives, John Phillips, Nina Paddu, Gitanjali Srivastava, Ronit Marom, Farah Ladha, Claudia Soler-Alfonso, Rachel Franciskovich, Mary Koziura, Deanna Bell, Sumit Pruthi, Thomas Cassini

    Published 2025-01-01
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