Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosomal in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinuria. [electronic resource]
Producer: 19920910Description: 296-304 p. digitalISSN:- 0007-1048
- Adult
- Anemia, Sideroblastic -- etiology
- Chromosomes, Human, Pair 8
- DNA -- analysis
- Erythrocytes -- ultrastructure
- Granulocytes -- ultrastructure
- Hemoglobinuria, Paroxysmal -- complications
- Histocytological Preparation Techniques
- Humans
- Immunohistochemistry
- Karyotyping
- Male
- Megakaryocytes -- ultrastructure
- Monocytes -- ultrastructure
- Nucleic Acid Hybridization
- Trisomy
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Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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