<--- Back to Details
First PageDocument Content
Health / Thalassemia / Beta-thalassemia / HBA2 / Hemoglobin E / Hemoglobin / HBD / HBB / Hereditary persistence of fetal hemoglobin / Hemoglobins / Medicine / Biology
Date: 2007-06-14 11:23:39
Health
Thalassemia
Beta-thalassemia
HBA2
Hemoglobin E
Hemoglobin
HBD
HBB
Hereditary persistence of fetal hemoglobin
Hemoglobins
Medicine
Biology

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update

Add to Reading List

Source URL: www.bx.psu.edu

Download Document from Source Website

File Size: 266,77 KB

Share Document on Facebook

Similar Documents

IMPC phenotyping SOPs in JMC Hematology IMPC_HEM_002 Purpose Hematological assessment of blood determines blood cell counts (white blood cells, red blood cells, hemoglobin, and platelets) and additional hematological par

DocID: 1vnKm - View Document

UCSF Benioff Children’s Hospital Oakland Northern California Comprehensive THALASSEMIA Center What is Thalassemia? Thalassemia is a genetic blood disorder that causes hemoglobin deficiency and

DocID: 1u2ik - View Document

HemaApp: Noninvasive Blood Screening of Hemoglobin using Smartphone Cameras

DocID: 1tG2U - View Document

A means of measuring total hemoglobin in the blood using a smartphone’s camera and flash. Many health conditions — such as anemia, malnutrition and pulmonary illnesses — impact hemoglobin levels. This app is not on

DocID: 1sYgE - View Document

Diabetes Self-Management Plan Your Hemoglobin A1c (HgbA1c) goal: Your blood sugar range target:

DocID: 1rBhz - View Document