βS haplotypes, α-globin gene status, and hematological data of sickle cell disease patients in Guadeloupe (F.W.I.)

Hemoglobin

Volumn 20, Issue 1, 1996, Pages 63-74

  Keclard L ^a   Ollendorf, V ^a   Berchel, C ^a   Loret, H ^b   Merault G ^a  

^a CHRU Pointe Pitre   (Guadeloupe)

^b Ctr Integre de la Drepanocytose   (Guadeloupe)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; HEMOGLOBIN S;

ALPHA THALASSEMIA; ARTICLE; BETA THALASSEMIA; CARIBBEAN ISLANDS; GENE CLUSTER; GENE FREQUENCY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; SENEGAL; SICKLE CELL ANEMIA;

ADOLESCENT; ALPHA-THALASSEMIA; ANEMIA, SICKLE CELL; CHILD; FEMALE; FETAL HEMOGLOBIN; GLOBINS; GUADELOUPE; HAPLOTYPES; HEMATOLOGIC TESTS; HUMANS; MALE; MULTIGENE FAMILY;

EID: 0029670772     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.3109/03630269609027911     Document Type: Article

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