首页> 外文OA文献 >Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism

【2h】

Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism

机译：Kallmann综合征分子诊断和Normosmic特发恶血症性低因素的靶向基因面板测序

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
相似文献
相关主题

著录项

作者
Ja Hye Kim; Go Hun Seo; Gu-Hwan Kim; Juyoung Huh; Il Tae Hwang; Ja-Hyun Jang; Han-Wook Yoo; Jin-Ho Choi;
展开▼
作者单位

展开▼
年度 2018
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献
中文文献
专利

1. Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism [J] . Kim Ja Hye, Seo Go Hun, Kim Gu-Hwan, Experimental and clinical endocrinology and diabetes: Official journal, German Society of Endocrinology [and] German Diabetes Association . 2019 ,第8期

机译：Kallmann综合征分子诊断的靶向基因面板测序和Normosmic特发性低血管性腺病药
2. Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome [J] . Quaynor Samuel D., Bosley Maggie E., Duckworth Christina G., Molecular and Cellular Endocrinology . 2016 ,第3期

机译：有针对性的下一代测序方法确定了正常性性腺功能减退性腺功能减退症和Kallmann综合征的18个新候选基因
3. Clinical, endocrinological, and molecular genetic characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism in childhood and adolescence [J] . Sun-Jeong Shin, Ja Hye Kim, Ja Hyang Cho, International journal of pediatric endocrinology . 2015 ,第Suppla1期

机译：儿童和青少年的Kallmann综合征和常态性特发性促性腺激素性性腺功能减退症的临床，内分泌和分子遗传学特征
4. Genetic Testing of Idiopathic Metabolic Disorders by Targeted Next-Generation Sequencing [C] . Catarina Silveira, A. M. Coutinho, J. Tavares, International Molecular Medicine Tri-Conference. . 2016

机译：靶向下一代测序的特发性代谢障碍的遗传检测
5. Next generation sequencing panels for the evaluation of colorectal cancer and polyposis syndromes: a cost-effectiveness analysis [D] . Gallego, Carlos J. 2014

机译：用于评估结直肠癌和息肉综合征的下一代测序面板：成本效益分析
6. Clinical endocrinological and molecular genetic characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism in childhood and adolescence [O] . Sun-Jeong Shin, Ja Hye Kim, Ja Hyang Cho, 2015

机译：儿童和青少年的Kallmann综合征和常态性特发性促性腺激素性性腺功能减退症的临床内分泌和分子遗传学特征
7. Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome [O] . Samuel D. Quaynor, Maggie E. Bosley, Christina G. Duckworth, 2016

机译：靶向的下一代测序方法识别Normosmic低因素性腺性腺性腺和Kallmann综合征中的十八个新候选基因

Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism

著录项

相似文献

相关主题

期刊订阅