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Volumn 28, Issue 2, 2008, Pages 165-166
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A case of transfusion-dependent nondeletional Hb H disease undiagnosed during prenatal screening for thalassemia
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Author keywords
thalassemia; Double heterozygotes; Hb constant spring; Nondeletional mutations
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Indexed keywords
ALPHA GLOBIN;
HEMOGLOBIN H;
ALPHA THALASSEMIA;
ANEMIA;
ARTICLE;
BLOOD TRANSFUSION;
CASE REPORT;
FAMILY HISTORY;
FETUS;
FIRST TRIMESTER PREGNANCY;
GENE DELETION;
GENETIC SCREENING;
HEMOGLOBIN H DISEASE;
HEPATOSPLENOMEGALY;
HUMAN;
MALE;
POLYMERASE CHAIN REACTION;
PRENATAL SCREENING;
PRIORITY JOURNAL;
ALPHA-THALASSEMIA;
BLOOD TRANSFUSION;
FEMALE;
GLOBINS;
HEMOGLOBINS, ABNORMAL;
HETEROZYGOTE DETECTION;
HUMANS;
INFANT;
INFANT, NEWBORN;
MALE;
POLYMERASE CHAIN REACTION;
PREGNANCY;
PRENATAL DIAGNOSIS;
THALASSEMIA;
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EID: 39749145025
PISSN: 01973851
EISSN: 10970223
Source Type: Journal
DOI: 10.1002/pd.1947 Document Type: Article |
Times cited : (9)
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References (9)
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