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Volumn 17, Issue 2, 2015, Pages 125-130
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State-based surveillance for selected hemoglobinopathies
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Author keywords
Hemoglobinopathies; Newborn screening; Sickle cell disease; Surveillance; Thalassemia
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Indexed keywords
AFRICAN AMERICAN;
AGE DISTRIBUTION;
ALPHA THALASSEMIA;
ARTICLE;
BETA THALASSEMIA;
BLACK PERSON;
DATA COLLECTION METHOD;
DISEASE SURVEILLANCE;
ETHNIC DIFFERENCE;
FEMALE;
HEMOGLOBIN H DISEASE;
HEMOGLOBIN SC DISEASE;
HEMOGLOBINOPATHY;
HUMAN;
INFORMATION PROCESSING;
MAJOR CLINICAL STUDY;
MALE;
PILOT STUDY;
RACE DIFFERENCE;
SEX DIFFERENCE;
SICKLE CELL ANEMIA;
SICKLE CELL BETA THALASSEMIA;
STATE BASED SURVEILLANCE SYSTEM;
THALASSEMIA;
THALASSEMIA INTERMEDIA;
THALASSEMIA MAJOR;
UNITED STATES;
ANEMIA, SICKLE CELL;
GENETICS;
HEALTH SURVEY;
HEMOGLOBINOPATHIES;
PREVALENCE;
REGISTER;
ANEMIA, SICKLE CELL;
FEMALE;
HEMOGLOBINOPATHIES;
HUMANS;
MALE;
POPULATION SURVEILLANCE;
PREVALENCE;
REGISTRIES;
THALASSEMIA;
UNITED STATES;
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EID: 84961290948
PISSN: 10983600
EISSN: 15300366
Source Type: Journal
DOI: 10.1038/gim.2014.81 Document Type: Article |
Times cited : (35)
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References (10)
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