Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Syndrome and ANTXR2[original query] |
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| The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series. BMC medical genetics 2018 May 19 (1): 87. Youssefian Leila, Vahidnezhad Hassan, Touati Andrew, Ziaee Vahid, Saeidian Amir Hossein, Pajouhanfar Sara, Zeinali Sirous, Uitto Jou |
| Genetic, clinical and biochemical characterization of a large cohort of patients with hyaline fibromatosis syndrome. Orphanet journal of rare diseases 2019 8 14 (1): 209. Cozma Claudia, Hovakimyan Marina, Iura?cu Marius-Ionu?, Makhseed Nawal, Selim Laila A, Alhashem Amal M, Ben-Omran Tawfeg, Mahmoud Iman G, Al Menabawy Nihal M, Al-Mureikhi Mariam, Martin Magi, Demuth Laura, Yüksel Zafer, Beetz Christian, Bauer Peter, Rolfs Arn |
| A Case of Hyaline Fibromatosis Syndrome with a New Variant of Genetic Mutation in ANTXR2 Gene. Annals of dermatology 2021 4 31 (Suppl): S12-S13. Park Chan Seong, Lee Jongeun, Byun Hyun Jeong, Lim Youngkyoung, Park Ji-Hye, Lee Jong Hee, Lee Dong-Youn, Lee Joo-Heung, Yang Jun-Mo, Lee Jee Hun, Yoo So-You |
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