TY - GEN AU - SCOTT,J L AU - HAUT,A AU - CARTWRIGHT,G E AU - WINTROBE,M M TI - Congenital hemolytic disease associated with red cell inclusion bodies, abnormal pigment metabolism and an electrophoretic hemoglobin abnormality SN - 0006-4971 PY - 1998///1101 KW - Anemia KW - Anemia, Hemolytic KW - Erythrocytes KW - Hemoglobins KW - Humans KW - Inclusion Bodies KW - Medical Records KW - Pigments, Biological KW - metabolism N1 - Publication Type: Case Reports; Journal Article ER -