Sickle beta thalassemia
A heterozygous state in which a person has a hemoglobin S allele along with a beta-thalassemia allele. The severity of the condition is determined to a large extent by the quantity of normal hemoglobin produced by the beta-thalassemia gene.
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Top doctors who continously share their opinions on Sickle beta thalassemiaEx.central Hospital Dhanbad.1985 ..1993..ex.pathologist .drs Tribedy and Roy Dianostic Lab.kolkata.ex Pathologist.inst of Child Health Kolkata.
Senior Pathologist
School of Tropical Medicine. Kolkata
d c p
Tata Central Hospital, Jamadoba
Consultant Pathologist
SCBMC, Cuttack, Orissa
MD(Pathology)
LLRM
Senior Resident
Dr. D. Y. Patil Medical College, Hospital & Research Centre
Assistant Professor In Hematology
Tata Medical Center
Bone marrow Transplant Fellowship
Apex Diagnostics
Consultant Pathologist
Gauhati Medical College
MBBS ,MD (Pathology)
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