Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta (vol 23, pg 1112, 2015)

Lindahl Katarina; Astroem Eva; Rubin Carl-Johan; Grigelioniene Giedre; Malmgren Barbro; Ljunggren Oesten; Kindmark Andreas

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Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta (vol 23, pg 1112, 2015)

机译：瑞典人群中成骨不全的遗传流行病学，患病率和基因型与表型的相关性（2015年第23卷，第1112页）

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《European journal of human genetics: EJHG》 |2015年第8期|共1页
作者
Lindahl Katarina; Astroem Eva; Rubin Carl-Johan; Grigelioniene Giedre; Malmgren Barbro; Ljunggren Oesten; Kindmark Andreas;
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正文语种 eng
中图分类医学遗传学;
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入库时间 2022-08-18 10:56:58

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1. Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta (vol 23, pg 1112, 2015) [J] . Lindahl Katarina, Astroem Eva, Rubin Carl-Johan, European journal of human genetics: EJHG . 2015,第8期

机译：瑞典人群中成骨不全的遗传流行病学，患病率和基因型与表型的相关性（2015年第23卷，第1112页）
2. Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta [J] . Lindahl Katarina, Astrom Eva, Rubin Carl-Johan, European journal of human genetics: EJHG . 2015,第8期

机译：遗传性流行病学，患病率和基因型与表型的相关性在瑞典人群中成骨不全
3. Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta (vol 30, pg 2333, 2019) [J] . Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA . 2020,第6期

机译：使用靶向下一代测序和基因型 - 表型相关性的综合遗传分析在53例日本骨质骨质术患者中（Vol 30，PG 2333,2019）
4. Allele frequencies for STR loci in a Sicilian population: Genetic prevalence and disequilibrium [C] . I. China, M. Guarnaccia, E. Ginestr, International Society for Forensic Genetics . 2006

机译：西西里人群中Str基因座的等位基因频率：遗传流行和不平衡
5. Recessive Osteogenesis Imperfecta: Prevalence and Pathophysiology of Collagen Prolyl 3-Hydroxylation Complex Defects [D] . Cabral, Wayne Anthony 2014

机译：隐性成骨不全：胶原蛋白脯氨酰3-羟基化复合物缺陷的患病率和病理生理学
6. Genetic epidemiology prevalence and genotype–phenotype correlations in the Swedish population with osteogenesis imperfecta [O] . Katarina Lindahl, Eva Åström, Carl-Johan Rubin, 2015

机译：瑞典人群成骨不全症的遗传流行病学患病率以及基因型与表型的相关性
7. Correction to: Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta [O] . Y. Ohata, S. Takeyari, Y. Nakano, 2020

机译：校正：使用靶向下一代测序的综合遗传分析和53例日本骨质骨质患者患者的靶向下一代测序和基因型表型相关性

Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta (vol 23, pg 1112, 2015)

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