TY  - GEN
AU  - Callen,D F
TI  - Alternative interpretation of reported paracentric inversion
SN  - 0002-9297
PY  - 1998///0813
KW  - Chromosome Aberrations
KW  - genetics
KW  - Chromosome Breakage
KW  - Chromosome Disorders
KW  - Chromosome Inversion
KW  - Chromosomes, Human, Pair 17
KW  - Crossing Over, Genetic
KW  - Gene Deletion
KW  - Genetic Markers
KW  - Humans
KW  - Karyotyping
KW  - Recombination, Genetic
N1  - Publication Type: Letter
UR  - https://doi.org/10.1086/301902
ER  -