Lisätietoja julkaisusta saa klikkaamalla sen numeroa.
For full details, please click the number in front of the publication.
|
1 |
Aikio O et al. |
Identtiset kolmoset, ihme kerrassaan.
|
|
2 |
Myllylä RM et al. |
Multiple miliary osteotoma cutis is a distinct disease entity: four case reports and review of the literature.
|
|
3 |
Nissi R et al. |
Hereditary isolated metatarsophalangeal arthritis.
|
|
4 |
Peippo M, Ignatius J. |
Pitt-Hopkins syndrome.
|
|
5 |
Siggberg L et al. |
Familial 6p22.2 duplication associates with mild developmental delay and increased SSADH activity.
|
|
6 |
Siggberg L et al. |
9q22 deletion - first familial case.
|