Heterozygosity at the alpha-haptoglobin locus associated with a deletion, 16q22 leads to 16qter
Cytogenet Cell Genet
.
1978;22(1-6):513.
doi: 10.1159/000131011.
Authors
M A Ferguson-Smith
,
D A Aitken
PMID:
752532
DOI:
10.1159/000131011
No abstract available
MeSH terms
Child
Chromosome Deletion*
Chromosome Mapping*
Chromosomes, Human, 16-18*
Female
Haptoglobins / genetics*
Heterozygote
Humans
Substances
Haptoglobins