Clinical, endocrinological, and molecular genetic characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism in childhood and adolescence

Sun-Jeong Shin; Ja Hye Kim; Ja Hyang Cho; Jae Hyun Kim; Gu-Hwan Kim; Jin-Ho Choi; Han-Wook Yoo

首页> 外文期刊>International journal of pediatric endocrinology >Clinical, endocrinological, and molecular genetic characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism in childhood and adolescence

【24h】

Clinical, endocrinological, and molecular genetic characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism in childhood and adolescence

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

获取原文

获取外文期刊封面封底 >>

开具论文收录证明 >>

文献代查 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《International journal of pediatric endocrinology》 |2015年第1期|共页
作者
Sun-Jeong Shin; Ja Hye Kim; Ja Hyang Cho; Jae Hyun Kim; Gu-Hwan Kim; Jin-Ho Choi; Han-Wook Yoo;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种
中图分类内分泌腺疾病及代谢病;
关键词

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. Molecular analysis of KAL-1 in a series of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism patients from Northwestern China [J] . Kai-Fa Tang, Qi-Fei Wu, Tie-Jun Zou, 亚洲男性学杂志：英文版 . 2009,第006期

机译：西北地区一系列卡尔曼综合征和常态性性腺功能减退性腺功能减退症患者KAL-1的分子分析
3. Novel FGFR1 mutations in Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: evidence for the involvement of an alternatively spliced isoform [J] . Goncalves Catarina, Bastos Margarida, Pignatelli Duarte, Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society . 2015,第5期

机译：Kallmann综合征中的新FGFR1突变和常态性特发性性腺功能低下性腺功能减退：另一种剪接同工型参与的证据
4. CLINICAL, GENETIC, MOLECULAR, AND CELLULAR ASPECTS OF THE BRUGADA SYNDROME [C] . CHARLES ANTZELEVITC International Congress on Electrocardiology . 2005

机译：Brugada综合征的临床，遗传，分子和细胞方面
5. Clinical investigation of the major and minor salivary glands in patients with autoimmune diseases (Sjogren's syndrome and idiopathic inflammatory myopathies) and in patients wearing complete dentures (Hungarian text). [D] . Marton, Krisztina. 2005

机译：自身免疫性疾病患者（干燥综合征和特发性炎症性肌病）和全口假牙患者的唾液腺的主要和次要的临床研究（匈牙利文）。
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. Clinical, endocrinological, and molecular genetic characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism in childhood and adolescence [O] . 2015

机译：儿童和青少年期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

Clinical, endocrinological, and molecular genetic characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism in childhood and adolescence

著录项

相似文献

相关主题

期刊订阅