Human Genome Epidemiology Literature Finder
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Query Trace: Osteogenesis Imperfecta and IFITM5[original query] |
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Osteogenesis imperfecta type V: Genetic and clinical findings in eleven Chinese patients. Clinica chimica acta; international journal of clinical chemistry 2016 Nov 462 201-209. Liu Yi, Wang Jiawei, Ma Doudou, Lv Fang, Xu Xiaojie, Xia Weibo, Jiang Yan, Wang Ou, Xing Xiaoping, Zhou Peiran, Wang Jianyi, Yu Wei, , Li M |
Extremely low level of serum pigment epithelium-derived factor is a special biomarker of Chinese osteogenesis imperfecta patients with SERPINF1 mutations. Clinica chimica acta; international journal of clinical chemistry 2018 Mar 478 216-221. Wang Jian-Yi, Li Lu-Jiao, Zhang Qian, Liu Yi, Lv Fang, Xu Xiao-Jie, Song Yu-Wen, Wang Ou, Jiang Yan, Xia Wei-Bo, Xing Xiao-Ping, Li M |
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 |
Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta. Bone 2018 3 110 368-377. Mrosk Julia, Bhavani Gandham SriLakshmi, Shah Hitesh, Hecht Jochen, Krüger Ulrike, Shukla Anju, Kornak Uwe, Girisha Katta Moh |
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 |
Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2019 Jul . Ohata Y, Takeyari S, Nakano Y, Kitaoka T, Nakayama H, Bizaoui V, Yamamoto K, Miyata K, Yamamoto K, Fujiwara M, Kubota T, Michigami T, Yamamoto K, Yamamoto T, Namba N, Ebina K, Yoshikawa H, Ozono |
Expanding the Clinical Spectrum of Osteogenesis Imperfecta Type V: 13 Additional Patients and Review. Frontiers in endocrinology 2019 6 10 375. Cao Yang-Jia, Wei Zhe, Zhang Hao, Zhang Zhen-L |
Genotypic and Phenotypic Characteristics of 29 Patients With Rare Types of Osteogenesis Imperfecta: Average 5 Years of Follow-Up. Frontiers in genetics 2021 8 12 622078. Xi Lei, Zhang Hao, Zhang Zhen-L |
Genotype-Phenotype Relationship and Follow-up Analysis of a Chinese Cohort With Osteogenesis Imperfecta. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2022 May . Wei Shuoshuo, Yao Yangyang, Shu Meng, Gao Ling, Zhao Jiajun, Li Tianyou, Wang Yanzhou, Xu Ch |
Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patients. Orphanet journal of rare diseases 2023 9 18 (1): 295. Peikai Chen, Yapeng Zhou, Zhijia Tan, Yunzhi Lin, Daniel Li-Liang Lin, Jingwei Wu, Zeluan Li, Hiu Tung Shek, Jianbin Wu, Yong Hu, Feng Zhu, Danny Chan, Kenneth Man-Chee Cheung, Michael Kai-Tsun |
Genotype and Phenotype Correlation of Patients with Osteogenesis Imperfecta. The Journal of molecular diagnostics : JMD 2024 7 . Lamiya Aliyeva, Yasemin Denkboy Ongen, Erdal Eren, Mehmet Bartu Sarisozen, Adem Alemdar, Sehime G Temel, Sebnem Ozemri S |
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