Erondu–Cymet Syndrome kitap kapağı
Kitap başlığı:

Erondu–Cymet Syndrome

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

Cede Publishing (2012-03-06 )

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ISBN-13:

978-620-0-83887-2

ISBN-10:
6200838879
EAN:
9786200838872
Kitabın dili:
İngilizce
Özet:
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.
Yayınevi:
Cede Publishing
Websitesi:
http://www.alphascript-publishing.com
Düzenleyen:
Barnabas Cristóbal
Sayfa sayısı:
52
Yayın tarihi:
2012-03-06
Hisse:
Mevcut
Kategori:
Biyoloji
Fiyat:
268.25 HK$
Anahtar kelimeler:
karyotype, Down syndrome, Human Genome Project, Chromosome 21 (human), Tyler Cymet

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