相关实验视频

Updated: Jun 10, 2025

Neonatal Murine Cochlear Explant Technique as an In Vitro Screening Tool in Hearing Research
08:30

Neonatal Murine Cochlear Explant Technique as an In Vitro Screening Tool in Hearing Research

Published on: June 8, 2017

17.6K

遗传性听力损失:在英国引入R67大型基因组

Ahmed Fazili1, Hannah Blanchford2, Kostas Tsioulos2

  • 1St George's University of London, London, UK.

The Journal of laryngology and otology
|October 21, 2024
PubMed
概括

遗传性听力损失的诊断正在得到改善. 一个新的大型基因组 (R67) 能够更快地识别遗传原因,从而为这种慢性疾病提供更有效的临床管理.

关键词:
诊断技术 诊断技术 诊断技术遗传学 遗传学 遗传学 是一个听力损失 听力损失是什么内耳的内耳是内耳的内耳.耳学 耳学 耳学感应神经神经听力损失

更多相关视频

FISH for Pre-implantation Genetic Diagnosis07:34

FISH for Pre-implantation Genetic Diagnosis

Published on: February 23, 2011

36.8K
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

8.6K

相关概念视频

Pleiotropy01:33

Pleiotropy

Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.0K