Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Disease and SERPINF1[original query] |
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| Genotype-phenotype correlation among Malaysian patients with osteogenesis imperfecta. Clinica chimica acta; international journal of clinical chemistry 2018 5 484 141-147. Mohd Nawawi Nadiah, Selveindran Nalini M, Rasat Rahmah, Chow Yock Ping, Abdul Latiff Zarina, Syed Zakaria Syed Zulkifli, Jamal Rahman, Abdul Murad Nor Azian, Abd Aziz Bilkis Ba |
| Genotype and malocclusion in patients with osteogenesis imperfecta. Orthodontics & craniofacial research 2018 2 21 (2): 71-77. Jabbour Z, Al-Khateeb A, Eimar H, Retrouvey J M, Rizkallah J, Glorieux F H, Rauch F, Tamimi |
| Osteogenesis imperfecta in Brazilian patients. Genetics and molecular biology 2019 8 42 (2): 344-350. Trancozo Maira, Moraes Marcos V D, Silva Dalila A, Soares Jéssica A M, Barbirato Clara, Almeida Márcio G, Santos Lígia R, Rebouças Maria R G O, Akel Akel N, Sipolatti Valentim, Nunes Vanda R R, Errera Flavia I V, Aguena Meire, Passos-Bueno Maria R, Paula Flavia |
| Insufficient evidence for a role of SERPINF1 in otosclerosis. Molecular genetics and genomics : MGG 2019 4 294 (4): 1001-1006. Valgaeren Hanne, Sommen Manou, Beyens Matthias, Vandeweyer Geert, Schrauwen Isabelle, Schepers Anne, Schatteman Isabelle, Topsakal Vedat, Dhooge Ingeborg, Kunst Henricus, Zanetti Diego, Huber Alexander M, Hoischen Alexander, Fransen Erik, Van Camp G |
| Genotype-phenotype relationship and comparison between eastern and western patients with osteogenesis imperfecta. Journal of endocrinological investigation 2023 6 . X Lin, J Hu, B Zhou, Q Zhang, Y Jiang, O Wang, W Xia, X Xing, M |
| Genetic variants and altered expression of SERPINF1 confer disease susceptibility in patients with otosclerosis. Journal of human genetics 2023 6 . Neha Singh, Kirtal Hansdah, Amal Bouzid, Chinmay Sundar Ray, Ashim Desai, Khirod Chandra Panda, Jyotish Chandra Choudhury, Adel Tekari, Saber Masmoudi, Puppala Venkat Ramchand |
| Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation. Journal of clinical research in pediatric endocrinology 2024 6 . Samim Özen, Damla Gök?en, Ferda Evin, Esra I??k, Hüseyin Onay, Bilça? Akgün, Aysun Ata, Tahir Atik, Füsun Düzcan, Ferda Özk?nay, ?ükran Darcan, Özgür Ço?u |
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