Molecular spectrum of alpha-thalassemia mutations in microcytic hypochromic anemia patients from Saudi Arabia.

Genetic testing and molecular biomarkers

Volumn 13, Issue 2, 2009, Pages 219-221

  Hellani, Ali ^a   Fadel, Elias ^a   El Sadadi, Shaker ^a   El Sweilam, Hamdan ^a   El Dawood, Ahmed ^a   Abu Amero, Khaled K ^a  

^a SAAD SPECIALIST HOSPITAL   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; HEMOGLOBIN H; POLYADENYLIC ACID;

ALPHA THALASSEMIA; ARTICLE; BLOOD; GENETIC SCREENING; GENETICS; GEOGRAPHY; HOMOZYGOTE; HUMAN; IRON DEFICIENCY ANEMIA; MUTATION; SAUDI ARABIA;

ALPHA-GLOBINS; ALPHA-THALASSEMIA; ANEMIA, HYPOCHROMIC; GENETIC SCREENING; GEOGRAPHY; HEMOGLOBIN H; HOMOZYGOTE; HUMANS; MUTATION; POLY A; SAUDI ARABIA;

EID: 67650022096     PISSN: None     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2008.0123     Document Type: Article

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