Mild hemoglobin H-constant spring disease with β-thalassemia - A case report

Annals of Hematology

Volumn 90, Issue 1, 2011, Pages 123-124

  Li, Dong Zhi ^a   Liao, Can ^a   Zhou, Jian Ying ^a   Xie, Xing Mei ^a   Li, Jian ^a  

^a GUANGZHOU MATERNAL AND NEONATAL HOSPITAL   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; FERRITIN; HEMOGLOBIN; HEMOGLOBIN A; HEMOGLOBIN A2; HEMOGLOBIN BART; HEMOGLOBIN F; HEMOGLOBIN H; HEMOGLOBIN H CONSTANT SPRING; UNCLASSIFIED DRUG;

ADULT; ALLELE; ALPHA THALASSEMIA; AMNIOCENTESIS; ANEMIA; BETA THALASSEMIA; BODY HEIGHT; BODY WEIGHT; CAPILLARY ELECTROPHORESIS; CASE REPORT; CELL INCLUSION; CODON; COINHERITANCE; ERYTHROCYTE COUNT; FEMALE; FETUS; GENE MUTATION; GENOTYPE; GLOBIN GENE; HEMOGLOBIN BLOOD LEVEL; HEMOGLOBIN H CONSTANT SPRING DISEASE; HEMOGLOBINOPATHY; HETEROZYGOTE; HOMOZYGOTE; HUMAN; INHERITANCE; LETTER; MALE; MEAN CORPUSCULAR HEMOGLOBIN; MEAN CORPUSCULAR VOLUME; MICROCYTOSIS; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SCREENING; SPOUSE; THALASSEMIA MAJOR;

ALPHA-THALASSEMIA; BETA-THALASSEMIA; FAMILY CHARACTERISTICS; FEMALE; HEMOGLOBINS, ABNORMAL; HUMANS; MALE; PREGNANCY; PREGNANCY COMPLICATIONS, HEMATOLOGIC; PRENATAL DIAGNOSIS;

EID: 78651304743     PISSN: 09395555     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00277-010-0955-8     Document Type: Letter

References (7)

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