TY  - GEN
AU  - Luna-Fineman,S
AU  - Shannon,K M
AU  - Lange,B J
TI  - Childhood monosomy 7: epidemiology, biology, and mechanistic implications
SN  - 0006-4971
PY  - 1995///0525
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Aberrations
KW  - epidemiology
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - Chromosomes, Human, Pair 7
KW  - Female
KW  - Genes, Neurofibromatosis 1
KW  - Genes, ras
KW  - Genetic Diseases, Inborn
KW  - genetics
KW  - Genetic Predisposition to Disease
KW  - Hematopoietic Stem Cells
KW  - pathology
KW  - Humans
KW  - Incidence
KW  - Infant
KW  - Infant, Newborn
KW  - Leukemia, Myeloid
KW  - classification
KW  - Leukemia, Radiation-Induced
KW  - Male
KW  - Monosomy
KW  - Myelodysplastic Syndromes
KW  - Neoplasms, Second Primary
KW  - chemically induced
KW  - Risk
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.; Review
ER  -