迪乔治综合征：发病机制复杂？也许是，也许不是。 - Suppr

Suppr

超能文献

DiGeorge syndrome: complex pathogenesis? Maybe, maybe not.

作者信息

Baldini A

出版信息

Mol Med Today. 2000 Jan;6(1):12. doi: 10.1016/s1357-4310(99)01627-5.

DOI:10.1016/s1357-4310(99)01627-5

PMID:10637568

Abstract

摘要

相似文献

DiGeorge syndrome: complex pathogenesis? Maybe, maybe not.

Mol Med Today. 2000 Jan;6(1):12. doi: 10.1016/s1357-4310(99)01627-5.

DiGeorge syndrome: an enigma in mice and men.

Mol Med Today. 2000 Jan;6(1):13-4. doi: 10.1016/s1357-4310(99)01641-x.

Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome.

Mol Med Today. 2000 Jan;6(1):10-1. doi: 10.1016/s1357-4310(99)01577-4.

Ubiquitination gene defect found in DiGeorge syndrome.

Mol Med Today. 1999 Jun;5(6):233. doi: 10.1016/s1357-4310(99)01491-4.

DiGeorge syndrome with discordant phenotype in monozygotic twins.

J Med Genet. 2000 Sep;37(9):E23. doi: 10.1136/jmg.37.9.e23.

Inherited t(9;22) as the cause of DiGeorge syndrome: a case report.

Malays J Pathol. 2009 Dec;31(2):133-6.

Deletion 22q11: spectrum of associated disorders.

Semin Pediatr Neurol. 2007 Sep;14(3):136-9. doi: 10.1016/j.spen.2007.07.005.

Genetics. Engineering a broken heart.

Nature. 1999 Sep 23;401(6751):335-7. doi: 10.1038/43804.

Deconstructing DiGeorge syndrome.

Nat Genet. 2001 Mar;27(3):238-40. doi: 10.1038/85784.

Getting to the heart of DiGeorge syndrome.

Nat Med. 1999 Oct;5(10):1120-1. doi: 10.1038/13438.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

相似文献

DiGeorge syndrome: complex pathogenesis? Maybe, maybe not.

Mol Med Today. 2000 Jan;6(1):12. doi: 10.1016/s1357-4310(99)01627-5.

DiGeorge syndrome: an enigma in mice and men.

Mol Med Today. 2000 Jan;6(1):13-4. doi: 10.1016/s1357-4310(99)01641-x.

Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome.

Mol Med Today. 2000 Jan;6(1):10-1. doi: 10.1016/s1357-4310(99)01577-4.

Ubiquitination gene defect found in DiGeorge syndrome.

Mol Med Today. 1999 Jun;5(6):233. doi: 10.1016/s1357-4310(99)01491-4.

DiGeorge syndrome with discordant phenotype in monozygotic twins.

J Med Genet. 2000 Sep;37(9):E23. doi: 10.1136/jmg.37.9.e23.

Inherited t(9;22) as the cause of DiGeorge syndrome: a case report.

Malays J Pathol. 2009 Dec;31(2):133-6.

Deletion 22q11: spectrum of associated disorders.

Semin Pediatr Neurol. 2007 Sep;14(3):136-9. doi: 10.1016/j.spen.2007.07.005.

Genetics. Engineering a broken heart.

Nature. 1999 Sep 23;401(6751):335-7. doi: 10.1038/43804.

Deconstructing DiGeorge syndrome.

Nat Genet. 2001 Mar;27(3):238-40. doi: 10.1038/85784.

Getting to the heart of DiGeorge syndrome.

Nat Med. 1999 Oct;5(10):1120-1. doi: 10.1038/13438.