Human Genome Epidemiology Literature Finder
|
Records 1 - 5 (of 5 Records) |
| Query Trace: Syndrome and ELANE[original query] |
|---|
| Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia. British journal of haematology 2009 Nov 147 (4): 535-42. Xia Jun, Bolyard Audrey A, Rodger Elin, Stein Steve, Aprikyan Andrew A, Dale David C, Link Daniel |
| Role of CSF3R mutations in the pathomechanism of congenital neutropenia and secondary acute myeloid leukemia. Annals of the New York Academy of Sciences 2016 Apr 1370 (1): 119-25. Klimiankou Maksim, Mellor-Heineke Sabine, Zeidler Cornelia, Welte Karl, Skokowa Jul |
| Utility of a targeted next-generation sequencing-based genetic screening panel in patients with periodic fever, aphthous stomatitis, pharyngitis, and adenitis syndrome. Archives of rheumatology 2023 9 38 (2): 299-306. Rabia Miray K??la Ekinci, Özlem Anla?, Özge Öza |
| Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel. European journal of haematology 2024 4 . Lital Yeshareem, Joanne Yacobovich, Asaf Lebel, Sharon Noy-Lotan, Orly Dgany, Tanya Krasnov, Galit Berger Pinto, Nino Oniashvili, Jacques Mardoukh, Bella Bielorai, Ruth Laor, Noa Mandel-Shorer, Ayelet Ben Barak, Carina Levin, Mahdi Asleh, Hagit Miskin, Shoshana Revel-Vilk, Dror Levin, Marganit Benish, Tsila Zuckerman, Ofir Wolach, Idit Pazgal, Dafna Brik Simon, Oded Gilad, Asaf David Yanir, Tracie Alison Goldberg, Shai Izraeli, Hannah Tamary, Orna Steinberg-Shem |
| The ELANE rs17223045C/T and rs3761007G/A variants are protective factors against COVID-19. Biomolecules & biomedicine 2024 1 . José Manuel Fragoso, Gilberto Vargas-Alarcón, Ángel Emanuel Martínez-Flores, Isela Montufar-Robles, Rosa Elda Barbosa-Cobos, Gustavo Rojas-Velazco, Julian Ramírez-Bel |
- Page last reviewed:Feb 1, 2024
- Content source:

