医学文献 >>
  • 检索发现
  • 增强检索
知识库 >>
  • 临床诊疗知识库
  • 中医药知识库
评价分析 >>
  • 机构
  • 作者
默认
×
热搜词:
换一批
论文 期刊
取消
高级检索

检索历史 清除

A large cohort study of prenatal exome sequencing redefines diagnosis in fetal corpus callosum anomalies.

广告
第一作者: Delphine,Héron
第一单位: Clinical Genetics Unit, Referral Centers for Rare Diseases 'Intellectual Disabilities of Rare Causes' and 'Developmental Anomalies and Malformative Syndromes', APHP Sorbonne University, Pitié Salpêtrière Hospital, APHP, Paris 75013, France.
作者单位: Clinical Genetics Unit, Referral Centers for Rare Diseases 'Intellectual Disabilities of Rare Causes' and 'Developmental Anomalies and Malformative Syndromes', APHP Sorbonne University, Pitié Salpêtrière Hospital, APHP, Paris 75013, France. [1] Medical Genetics Department, Developmental and Reproductive Genomics Unit, APHP Sorbonne University, Pitié-Salpêtrière Hospital, APHP, Paris 75013, France. [2] Medical Genetics Department, Developmental and Reproductive Genomics Unit, APHP Sorbonne University, Pitié-Salpêtrière Hospital, APHP, Paris 75013, France.;Paris Brain Institute, Sorbonne Université, Inserm U1127, CNRS UMR 7225, Hôpital Pitié-Salpêtrière, Paris 75013, France. [3] Department of Pediatric Radiology, Trousseau Hospital, AP-HP.Sorbonne University, Paris 75012, France. [4] Pediatric Neurology Department, Timone Enfant, APHM, Marseille 13005, France. [5] Department of Radiology, University Hospital Timone, Aix Marseille University, Marseille 13005, France. [6] Department of Child Neurology, Referral Centers for Rare Diseases 'Intellectual Disabilities of Rare Causes', Lyon Hospital, and University Claude Bernard Lyon 1, Lyon 69500, France. [7] Department of Fetal and Pediatric Imaging, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Bron 69500, France. [8] Department of Medical Genetics, Purpan Hospital, CHU de Toulouse, Toulouse 31200, France. [9] Obstetrics and Gynaecology Department, Antoine Béclère Hospital, APHP, Paris Saclay University, Clamart 92140, France. [10] Neonatal and Pediatric Units, Louis-Mourier Hospital APHP, Colombes 92025, France. [11] Medical Genetics Unit, Nantes Hospital and University, Nantes 44000, France. [12] Department of Obstetrics and Gynecology, CHU Nantes, Nantes 44000, France. [13] Pediatric Neurology Department, Referral Centers for Rare Diseases 'Intellectual Disabilities of Rare Causes', APHP Sorbonne University, Armand Trousseau Hospital, APHP, Paris 75012, France. [14] CPDPN, Pôle mère enfant, Maison de Santé Protestante Bordeaux Bagatelle, Talence 33522, France. [15] Department of Obstetric, Cochin Hospital, APHP, Université Paris Cité, Paris 75014, France. [16] Fetal Medicine Department, Armand Trousseau University Hospital, DMU Origyne, Sorbonne University, Paris 75012, France. [17]
DOI 10.1093/brain/awaf311
PMID 40905141
发布时间 2025-12-04
提交
  • 浏览0
Brain : a journal of neurology

相似文献

  • 中文期刊
  • 外文期刊
  • 学位论文
  • 会议论文

加载中!

加载中!

加载中!

加载中!

法律状态公告日 法律状态 法律状态信息

特别提示:本网站仅提供医学学术资源服务,不销售任何药品和器械,有关药品和器械的销售信息,请查阅其他网站。

  • 客服热线:4000-115-888 转3 (周一至周五:8:00至17:00)

  • |
  • 客服邮箱:yiyao@wanfangdata.com.cn

  • 违法和不良信息举报电话:4000-115-888,举报邮箱:problem@wanfangdata.com.cn,举报专区

官方微信
万方医学小程序
new医文AI 翻译 充值 订阅 收藏 移动端

官方微信

万方医学小程序

使用
帮助
Alternate Text
调查问卷