TY  - GEN
AU  - Petit,P
AU  - Van den Berghe,H
TI  - A chromosomal abnormality (21q-) in primary thrombocytosis
SN  - 0340-6717
PY  - 1979///1024
KW  - Aged
KW  - Chromosome Deletion
KW  - Chromosomes, Human, 21-22 and Y
KW  - Female
KW  - Humans
KW  - Thrombocytosis
KW  - genetics
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1007/BF00295597
ER  -