TY  - GEN
AU  - Parlier,V
AU  - Tiainen,M
AU  - Beris,P
AU  - Miescher,P A
AU  - Knuutila,S
AU  - Jotterand Bellomo,M
TI  - 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
SN  - 0007-1048
PY  - 1992///0910
KW  - Adult
KW  - Anemia, Sideroblastic
KW  - etiology
KW  - Chromosomes, Human, Pair 8
KW  - DNA
KW  - analysis
KW  - Erythrocytes
KW  - ultrastructure
KW  - Granulocytes
KW  - Hemoglobinuria, Paroxysmal
KW  - complications
KW  - Histocytological Preparation Techniques
KW  - Humans
KW  - Immunohistochemistry
KW  - Karyotyping
KW  - Male
KW  - Megakaryocytes
KW  - Monocytes
KW  - Nucleic Acid Hybridization
KW  - Trisomy
N1  - Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1365-2141.1992.tb08223.x
ER  -