Kallmann syndrome associated with complex chromosome rearrangement
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference17 articles.
1. X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome
2. Hypogonadotropic Hypogonadism and Anosmia (Kallmann's Syndrome) Associated with a Marker Chromosome
3. Chromosome abnormality in Kallmann syndrome
4. Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletion
5. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
Cited by 17 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Hypergonadotropic hypogonadism and chromosomal aberrations: clinical heterogeneity and implications on the health of elderly men, case series;BMC Endocrine Disorders;2023-05-17
2. Genetic Diagnosis of Hypogonadotropic Hypogonadism and Kallmann Syndrome;Genetic Diagnosis of Endocrine Disorders;2010
3. Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance;Clinical Genetics;2008-06-28
4. Clinical Manifestations of Impaired GnRH Neuron Development and Function;Neurosignals;2008
5. Renal dysgenesis and KAL1 gene defects in patients with sporadic Kallmann syndrome;Fertility and Sterility;2007-11
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3