Human Genome Epidemiology Literature Finder
|
Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and PCNT[original query] |
|---|
| A Genetic Study of Psychosis in Huntington's Disease: Evidence for the Involvement of Glutamate Signaling Pathways. Journal of Huntington's disease 2018 7 (1): 51-59. Tsuang Debby W, Greenwood Tiffany A, Jayadev Suman, Davis Marie, Shutes-David Andrew, Bird Thomas |
| Exome sequencing in 38 patients with intracranial aneurysms and subarachnoid hemorrhage. Journal of neurology 2020 May . Sauvigny Thomas, Alawi Malik, Krause Linda, Renner Sina, Spohn Michael, Busch Alice, Kolbe Verena, Altmüller Janine, Löscher Britt-Sabina, Franke Andre, Brockmann Christian, Lieb Wolfgang, Westphal Manfred, Schmidt Nils Ole, Regelsberger Jan, Rosenberger Geo |
| Ciliary phenotyping in renal epithelial cells in a cranioectodermal dysplasia patient with WDR35 variants. Frontiers in molecular biosciences 2024 1 10 1285790. Joanna Walczak-Sztulpa, Anna Wawrocka, ?ukasz Kuszel, Paulina Pietras, Marta Le?niczak-Staszak, Miros?aw Andrusiewicz, Maciej R Krawczy?ski, Anna Latos-Biele?ska, Marta Pawlak, Ryszard Grenda, Anna Materna-Kiryluk, Machteld M Oud, Witold Szaflars |
| Reanalysis of Exome Sequencing Data in the Indian Undiagnosed Diseases Program: Improving Diagnostic Yield and Ending Diagnostic Odyssey. Clinical genetics 2025 1 . Neha Garg, Pragna Lakshmi, Suzena M Singh, Samarth Kulshreshta, Prajnya Ranganath, Amita Moirangthem, Ashwin Dalal, Aakanksha Gahlot, Ratna Dua Pu |
- Page last reviewed:Feb 1, 2024
- Content source:

