Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Osteogenesis Imperfecta and SERPINF1[original query] |
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Normal bone density and fat mass in heterozygous SERPINF1 mutation carriers. The Journal of clinical endocrinology and metabolism 2014 Nov 99 (11): E2446-50. Al-Jallad Hadil, Palomo Telma, Moffatt Pierre, Roughley Peter, Glorieux Francis H, Rauch Fra |
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 |
Co-occurrence of heterozygous mutations in COL1A1 and SERPINF1 in a high-risk pregnancy complicated by osteogenesis imperfecta. Journal of genetics 2019 6 98 (2): . Ji Yunpeng, Ikram Aqsa, Ma Zhongren, Peppelenbosch Maikel P, Pan Qiuw |
Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta. Frontiers in genetics 2020 10 11 984. Li Shan, Cao Yixuan, Wang Han, Li Lulu, Ren Xiuzhi, Mi Huan, Wang Yanzhou, Guan Yun, Zhao Feiyue, Mao Bin, Yang Tao, You Yi, Guan Xin, Yang Yujiao, Zhang Xue, Zhao Xiu |
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 |
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- Page last updated:May 13, 2024
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