Germline mutation in the STK11 gene in a girl with an ovarian Sertoli cell tumour
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00431-006-0352-4.pdf
Reference8 articles.
1. Hearle N, Schumacher V, Menko FH, Olschwang S, Boardman LA, Gille JJP, Josbert J, Keller JJ, Westerman AM, Scott RJ, Lim W, Trimbath JD, Giardiello FM, Gruber SB, Offerhaus GJA, de Rooij FWM, Wilson JHP, Hansmann A, Möslein G, Royer-Pokora B, Vogel T, Phillips RKS, Spigelman AD, Houlston RS (2006) Frequency and spectrum of cancers in the Peutz-Jeghers syndrome. Clin Cancer Res 12:3209–3215
2. Launonen V (2005) Mutations in the human LKB1/STK11 gene. Hum Mutat 26:291–297
3. McGarrity TJ, Kulin HE, Zaino RJ (2000) Peutz-Jeghers syndrome. Am J Gastroenterol 95:596–604
4. Oliva E, Alvarez T, Young RH (2005) Sertoli cell tumors of the ovary. A clinicopathologic and immunohistochemical study of 54 cases. Am J Surg Pathol 29:143–156
5. Sellner LN, Edkins E, Smith N (2006) Screening for RB1 mutations in tumor tissue using denaturing high performance liquid chromatography, multiplex ligation-dependent probe amplification, and loss of heterozygosity analysis. Pediatr Dev Pathol 9:31–37
Cited by 12 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. STK11 Adnexal Tumor: Exploring the Association With Peutz-Jeghers Syndrome and its Distinction From Morphologic Mimickers;Advances in Anatomic Pathology;2024-09-03
2. Diagnostic Conundrum of a Sertoli Cell Tumor in a 2-Year-Old Girl with Peripheral Precocious Puberty and a Café-au-Lait Macule: A Case Report;Hormone Research in Paediatrics;2024-04-16
3. Clinical Guidelines for Diagnosis and Management of Peutz-Jeghers Syndrome in Children and Adults;Digestion;2023
4. Delayed diagnosis of Peutz–Jeghers syndrome due to pathological information loss or mistake in family/personal history;Orphanet Journal of Rare Diseases;2021-06-08
5. Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panels;Genetics in Medicine;2019-07
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