TY  - GEN
AU  - Ferguson-Smith,M A
AU  - Aitken,D A
TI  - Heterozygosity at the alpha-haptoglobin locus associated with a deletion, 16q22 leads to 16qter
SN  - 0301-0171
PY  - 1979///0925
KW  - Child
KW  - Chromosome Deletion
KW  - Chromosome Mapping
KW  - Chromosomes, Human, 16-18
KW  - Female
KW  - Haptoglobins
KW  - genetics
KW  - Heterozygote
KW  - Humans
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1159/000131011
ER  -