TY  - GEN
AU  - Kotze,M J
AU  - Callis,M
TI  - Medped FH: a paradigm for other common monogenic diseases in South Africa
SN  - 0021-9150
PY  - 1999///0916
KW  - Child
KW  - Chromosome Aberrations
KW  - genetics
KW  - Chromosome Disorders
KW  - Genes, Dominant
KW  - Genetic Carrier Screening
KW  - Genetics, Population
KW  - Humans
KW  - Hyperlipoproteinemia Type II
KW  - Mutation
KW  - Receptors, LDL
KW  - South Africa
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1016/s0021-9150(99)00096-9
ER  -