|
🐜
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The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.
9 auth.
E. Tahvanainen,
S. Ranta,
Aune HIRVASNIEMId,
E. Karila,
J. Leisti,
P. Sistonen,
...
J. Weissenbach,
A. Lehesjoki,
A. Chapelle
|
6 |
1994 |
6
🐜
|
|
🐜
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Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis
7 auth.
E. Tahvanainen,
R. Norio,
E. Karila,
S. Ranta,
J. Weissenbach,
P. Sistonen,
...
A. Chapelle
|
6 |
1994 |
6
🐜
|
|
🐜
|
Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis.
8 auth.
E. Tahvanainen,
H. Forsius,
E. Karila,
S. Ranta,
M. Eerola,
J. Weissenbach,
...
P. Sistonen,
A. de la Chapelle
|
4 |
1995 |
4
🐜
|
|
🐜
|
Linkage disequilibrium mapping of the cornea plana congenita gene CNA2.
8 auth.
E. Tahvanainen,
H. Forsius,
M. Damsten,
E. Karila,
J. Kolehmainen,
J. Weissenbach,
...
P. Sistonen,
A. de la Chapelle
|
4 |
1995 |
4
🐜
|
|
🐢
|
A gene defect causing a novel progressive epilepsy with mental retardation, EPMR, maps to chromosome 8p
S. Ranta,
E. Tahvanainen,
E. Karila
|
1 |
1994 |
1
🐢
|
