Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and ALK[original query] |
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DHPLC-based mutation analysis of ENG and ALK-1 genes in HHT Italian population. Human mutation 2006 1 27 (2): 213-4. Lenato Gennaro M, Lastella Patrizia, Di Giacomo Marilena C, Resta Nicoletta, Suppressa Patrizia, Pasculli Giovanna, Sabbà Carlo, Guanti Ginev |
Impact of genotype and mutation type on health-related quality of life in patients with hereditary hemorrhagic telangiectasia. Acta oto-laryngologica 2009 Aug 129 (8): 862-6. Pfister Markus, Zalaman Ilse M, Blumenstock Gunnar, Mauz Paul-Stefan, Baumann In |
Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity Reactions.
Clinical pharmacology and therapeutics 2019 May . Nicoletti Paola, Barrett Sarah, McEvoy Laurence, Daly Ann K, Aithal Guruprasad, Lucena M Isabel, Andrade Raul J, Wadelius Mia, Hallberg Pär, Stephens Camilla, Bjornsson Einar S, Friedmann Peter, Kainu Kati, Laitinen Tarja, Marson Anthony, Molokhia Mariam, Phillips Elizabeth, Pichler Werner, Romano Antonino, Shear Neil, Sills Graeme, Tanno Luciana K, Swale Ashley, Floratos Aris, Shen Yufeng, Nelson Matthew R, Watkins Paul B, Daly Mark J, Morris Andrew P, Alfirevic Ana, Pirmohamed Mun |
Novel pathogenic alterations in pediatric and adult desmoid-type fibromatosis - A systematic analysis of 204 cases. Scientific reports 2020 Feb 10 (1): 3368. Trautmann Marcel, Rehkämper Jan, Gevensleben Heidrun, Becker Jessica, Wardelmann Eva, Hartmann Wolfgang, Grünewald Inga, Huss Sebasti |
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