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Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis. [electronic resource] by
- Datz, C
- Lalloz, M R
- Vogel, W
- Graziadei, I
- Hackl, F
- Vautier, G
- Layton, D M
- Maier-Dobersberger, T
- Ferenci, P
- Penner, E
- Sandhofer, F
- Bomford, A
- Paulweber, B
Producer: 19980212
In:
Journal of hepatology vol. 27
Availability: No items available.
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50.
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Molecular analysis of the genotype-phenotype relationship in factor X deficiency. [electronic resource] by
- Millar, D S
- Elliston, L
- Deex, P
- Krawczak, M
- Wacey, A I
- Reynaud, J
- Nieuwenhuis, H K
- Bolton-Maggs, P
- Mannucci, P M
- Reverter, J C
- Cachia, P
- Pasi, K J
- Layton, D M
- Cooper, D N
Producer: 20000413
In:
Human genetics vol. 106
Availability: No items available.
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51.
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Mutation of the von Hippel-Lindau gene alters human cardiopulmonary physiology. [electronic resource] by
- Smith, T G
- Brooks, J T
- Balanos, G M
- Lappin, T R
- Layton, D M
- Leedham, D L
- Liu, C
- Maxwell, P H
- McMullin, M F
- McNamara, C J
- Percy, M J
- Pugh, C W
- Ratcliffe, P J
- Talbot, N P
- Treacy, M
- Robbins, P A
Producer: 20080123
In:
Advances in experimental medicine and biology vol. 605
Availability: No items available.
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