1
|
Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19.
|
Hum Genet
|
1985
|
1.53
|
2
|
Homeobox genes and gut development.
|
Bioessays
|
2000
|
1.01
|
3
|
A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis.
|
Genomics
|
1990
|
0.85
|
4
|
The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22.
|
Ann Hum Genet
|
1987
|
0.79
|
5
|
A study of the structure of the gene for lecithin: cholesterol acyltransferase in four unrelated individuals with familial lecithin: cholesterol acyltransferase deficiency.
|
Clin Sci (Lond)
|
1988
|
0.75
|
6
|
[New therapeutic prospectives in Behçet's disease: beta-interferon].
|
Recenti Prog Med
|
1988
|
0.75
|
7
|
[Clinical experience in a case of chronic myeloid leukemia in accelerated phase treated with beta-interferon].
|
Recenti Prog Med
|
1989
|
0.75
|
8
|
[Pulmonary alveolar proteinosis].
|
Recenti Prog Med
|
1986
|
0.75
|
9
|
The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase).
|
Hum Genet
|
1985
|
0.75
|
10
|
[The appearance of a PNH clone during enzymopenic hemolytic anemia].
|
Clin Ter
|
1992
|
0.75
|
11
|
[Large-cell mediastinal lymphoma].
|
Clin Ter
|
1992
|
0.75
|