Erondu–Cymet Syndrome的封面
书籍主题:

Erondu–Cymet Syndrome

Chromosome 21 (human), Karyotype, Tyler Cymet, Down syndrome, Human Genome Project

Cede Publishing (2012-03-06 )

Books loader

Omni badge 有获得代金券的资格
ISBN-13:

978-620-0-83887-2

ISBN-10:
6200838879
EAN:
9786200838872
书籍语言:
英文
作品简介:
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Erondu–Cymet syndrome is a syndrome caused by a translocation on the . The genetic for people with this condition is 46, XY, inv(21)(q11.2q22.1). Findings in these patients include: hypotension, hypoxemia, seizures, and impairment of cognitive ability. Patients with this condition may have persistent left superior vena cava that drains into the left atrium, as well as pulmonary arterio-venous malformations. Erondu–Cymet Syndrome was discovered in 2006 by Ugochi Erondu and . In 2000, researchers working on the announced that they had determined the sequence of that make up this chromosome. Chromosome 21 was the second human chromosome to be fully sequenced.
出版社 :
Cede Publishing
网址:
http://www.alphascript-publishing.com
出版发行由:
Barnabas Cristóbal
页码 :
52
发表日期:
2012-03-06
现货:
备有现货
类别:
生物学
价格:
1,026.89 NT$
关键词:
karyotype, Down syndrome, Human Genome Project, Chromosome 21 (human), Tyler Cymet

Books loader

Adyen::diners Adyen::jcb Adyen::discover Adyen::cup Adyen::ach Adyen::unionpay Adyen::paypal Paypal

LOGIN
  0产品在购物车内
编辑购物车
Loading frontend
LOADING