| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Clinical genetics in transition—a comparison of genetic services in Estonia, Finland, and the Netherlands
|
Vrijenhoek, T.
|
|
|
12 |
2 |
p. 277-290
|
article
|
| 2 |
Curative gene therapies for rare diseases
|
Maldonado, Rocio
|
|
|
12 |
2 |
p. 267-276
|
article
|
| 3 |
European Reference Networks: challenges and opportunities
|
Tumiene, Birute
|
|
|
12 |
2 |
p. 217-229
|
article
|
| 4 |
Improving diagnostics of rare genetic diseases with NGS approaches
|
Vinkšel, Mateja
|
|
|
12 |
2 |
p. 247-256
|
article
|
| 5 |
Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide
|
Cornel, Martina C.
|
|
|
12 |
2 |
p. 257-265
|
article
|
| 6 |
Our greatest untapped resource: our patients
|
Bolz-Johnson, Matt
|
|
|
12 |
2 |
p. 241-246
|
article
|
| 7 |
Rare disease care pathways in the EU: from odysseys and labyrinths towards highways
|
Tumiene, Birute
|
|
|
12 |
2 |
p. 231-239
|
article
|
| 8 |
Rare diseases: past achievements and future prospects
|
Tumiene, Birute
|
|
|
12 |
2 |
p. 205-206
|
article
|
| 9 |
Shaping national plans and strategies for rare diseases in Europe: past, present, and future
|
Hedley, Victoria
|
|
|
12 |
2 |
p. 207-216
|
article
|
Journal description