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Updated: May 7, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

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

家族性胸大動脈動脈瘤および解剖: 5q13-14への主要な場所のマッピングを持つ遺伝的異質性

D Guo1, S Hasham, S Q Kuang

  • 1Department of Internal Medicine, University of Texas-Houston Medical School, Houston, TX 77030, USA.

Circulation
|May 23, 2001
PubMed
まとめ

家族性胸前大動脈動脈瘤および解剖 (TAA/解剖) の主要な遺伝子位置は,染色体5q13-14.4にマップされています. 媒介性ネクロシスのこの遺伝的原因は異質であり,一部の家族はこの場所とリンクしていない.

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Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information09:37

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information

Published on: August 15, 2019

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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