Homozygosity for the Mediterranean a-thalassemic deletion (hemoglobin Barts hydrops fetalis).

Annals of Saudi medicine

Volumn 30, Issue 2, 2010, Pages 153-155

  Al Allawi, Nasir A S ^a   Shamdeen, Maida Y ^b   Rasheed, Najeeb S ^b  

^a UNIVERSITY OF DUHOK   (Iraq)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN;

ADULT; ALPHA THALASSEMIA; ARTICLE; CASE REPORT; CONSANGUINITY; ECHOGRAPHY; FEMALE; FETUS HYDROPS; GENE DELETION; GENETICS; HOMOZYGOTE; HUMAN; MALE; NEWBORN; PHENOTYPE; PREGNANCY; STILLBIRTH; SYNDROME;

ALPHA-THALASSEMIA; CONSANGUINITY; FEMALE; GENE DELETION; HEMOGLOBINS; HOMOZYGOTE; HUMANS; HYDROPS FETALIS; INFANT, NEWBORN; MALE; PHENOTYPE; PREGNANCY; STILLBIRTH; SYNDROME; YOUNG ADULT;

MLCS; MLOWN;

EID: 77953050354     PISSN: None     EISSN: 09754466     Source Type: Journal    
DOI: 10.4103/0256-4947.60523     Document Type: Article

References (0)