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Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns. [electronic resource] by
- Piippo, K
- Laitinen, P
- Swan, H
- Toivonen, L
- Viitasalo, M
- Pasternack, M
- Paavonen, K
- Chapman, H
- Wann, K T
- Hirvelä, E
- Sajantila, A
- Kontula, K
Producer: 20000627
In:
Journal of the American College of Cardiology vol. 35
Availability: No items available.
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66.
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Neonatal serologic screening and early treatment for congenital Toxoplasma gondii infection. The New England Regional Toxoplasma Working Group. [electronic resource] by
- Guerina, N G
- Hsu, H W
- Meissner, H C
- Maguire, J H
- Lynfield, R
- Stechenberg, B
- Abroms, I
- Pasternack, M S
- Hoff, R
- Eaton, R B
Producer: 19940630
In:
The New England journal of medicine vol. 330
Availability: No items available.
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67.
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Retarded growth and deficits in the enteric and parasympathetic nervous system in mice lacking GFR alpha2, a functional neurturin receptor. [electronic resource] by
- Rossi, J
- Luukko, K
- Poteryaev, D
- Laurikainen, A
- Sun, Y F
- Laakso, T
- Eerikäinen, S
- Tuominen, R
- Lakso, M
- Rauvala, H
- Arumäe, U
- Pasternack, M
- Saarma, M
- Airaksinen, M S
Producer: 19990330
In:
Neuron vol. 22
Availability: No items available.
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