Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: HAX1[original query] |
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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 |
Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome. British journal of haematology 2009 May 145 (4): 533-4. Steinemann Doris, Praulich Inka, Otto Noreen, Göhring Gudrun, Niemeyer Charlotte M, Schlegelberger Brigit |
Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia. Haematologica 2010 1 95 (1): 168-9. Lanciotti Marina, Indaco Stefania, Bonanomi Sonia, Coliva Tiziana, Mastrodicasa Elena, Caridi Gianluca, Calvillo Michaela, Dufour Car |
Genome-wide meta-analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Apr . Yin Xianyong, Bizon Chris, Tilson Jeffrey, Lin Yuan, Gizer Ian R, Ehlers Cindy L, Wilhelmsen Kirk |
Genetic Polymorphisms in Activating Transcription Factor 3 Binding Site and the Prognosis of Early-Stage Non-Small Cell Lung Cancer. Oncology 2021 2 99 (5): 336-344. Kang Hyo-Gyoung, Park Ji Eun, Lee Shin Yup, Choi Jin Eun, Do Sook Kyung, Hong Mi Jeong, Lee Jang Hyuck, Jeong Ji Yun, Do Young Woo, Lee Eung Bae, Shin Kyung Min, Lee Won Ki, Choi Sun Ha, Lee Yong Hoon, Seo Hye Won, Yoo Seung Soo, Lee Jaehee, Cha Seung Ick, Kim Chang Ho, Cho Sukki, Jheon Sanghoon, Park Jae Yo |
HAX1-related congenital neutropenia: Long-term observation in paediatric and adult patients enrolled in the European branch of the Severe Chronic Neutropenia International Registry (SCNIR). British journal of haematology 2023 5 . Denys Pogozhykh, Deniz Yilmaz Karapinar, Maksim Klimiankou, Natali Gerschmann, Georg Ebetsberger-Dachs, Jan Palmblad, Göran Carlsson, Tania Masmas, Sally Kinsey, Marije Bartels, Sabine Mellor-Heineke, Karl Welte, Julia Skokowa, Cornelia Zeidl |
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 |
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- Page last updated:Apr 22, 2024
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