Results
|
1261.
|
|
|
1262.
|
|
|
1263.
|
|
|
1264.
|
|
|
1265.
|
|
|
1266.
|
|
|
1267.
|
|
|
1268.
|
|
|
1269.
|
|
|
1270.
|
The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy. [electronic resource] by
- Møller, Daniel Vega
- Pham, Tam Thanh
- Gustafsson, Finn
- Hedley, Paula
- Ersbøll, Mads Kristian
- Bundgaard, Henning
- Andersen, Claus B
- Torp-Pedersen, Christian
- Køber, Lars
- Christiansen, Michael
Producer: 20100325
In:
European journal of heart failure vol. 11
Availability: No items available.
|
|
1271.
|
Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa. [electronic resource] by
- Wang, Hui
- den Hollander, Anneke I
- Moayedi, Yalda
- Abulimiti, Abuduaini
- Li, Yumei
- Collin, Rob W J
- Hoyng, Carel B
- Lopez, Irma
- Abboud, Emad B
- Al-Rajhi, Ali A
- Bray, Molly
- Lewis, Richard Alan
- Lupski, James R
- Mardon, Graeme
- Koenekoop, Robert K
- Chen, Rui
Producer: 20090409
In:
American journal of human genetics vol. 84
Availability: No items available.
|
|
1272.
|
R27X nonsense mutation of the SDHB gene in a patient with sporadic malignant paraganglioma. [electronic resource] by
- Naito, Masaki
- Usui, Takeshi
- Tamanaha, Tamiko
- Kawashima, Sachiko-Tsukamoto
- Iogawa, Hitomi
- Hagiwara, Hanae
- Kimura, Takashi
- Tagami, Tetsuya
- Kurosawa, Manabu
- Shimatsu, Akira
- Naruse, Mitsuhide
Producer: 20091001
In:
Endocrine vol. 36
Availability: No items available.
|
|
1273.
|
|
|
1274.
|
|
|
1275.
|
|
|
1276.
|
|
|
1277.
|
|
|
1278.
|
|
|
1279.
|
|
|
1280.
|
|