Portada del libro de Erondu–Cymet Syndrome
Título del libro:

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
Idioma del libro:
Inglés
Notas y citas / Texto breve:
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.
Editorial:
Cede Publishing
Sitio web:
http://www.alphascript-publishing.com
Editado por:
Barnabas Cristóbal
Número de páginas:
52
Publicado en:
2012-03-06
Stock:
Disponible
Categoría:
Biología
Precio:
33.93 $
Palabras clave:
karyotype, Down syndrome, Human Genome Project, Chromosome 21 (human), Tyler Cymet

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