Results
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408281.
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408282.
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408283.
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408284.
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408285.
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408286.
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408287.
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Mutations in the human factor XII gene. [electronic resource] by
- Schloesser, M
- Zeerleder, S
- Lutze, G
- Halbmayer, W M
- Hofferbert, S
- Hinney, B
- Koestering, H
- Lämmle, B
- Pindur, G
- Thies, K
- Köhler, M
- Engel, W
Producer: 19971208
In:
Blood vol. 90
Availability: No items available.
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408288.
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Immunocytochemical diagnosis of acute promyelocytic leukemia (M3) with the monoclonal antibody PG-M3 (anti-PML). [electronic resource] by
- Falini, B
- Flenghi, L
- Fagioli, M
- Lo Coco, F
- Cordone, I
- Diverio, D
- Pasqualucci, L
- Biondi, A
- Riganelli, D
- Orleth, A
- Liso, A
- Martelli, M F
- Pelicci, P G
- Pileri, S
Producer: 19971208
In:
Blood vol. 90
Availability: No items available.
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408289.
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408290.
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408291.
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408292.
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408293.
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408294.
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408295.
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408296.
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KCNE1 mutations cause jervell and Lange-Nielsen syndrome. [electronic resource] by
- Schulze-Bahr, E
- Wang, Q
- Wedekind, H
- Haverkamp, W
- Chen, Q
- Sun, Y
- Rubie, C
- Hördt, M
- Towbin, J A
- Borggrefe, M
- Assmann, G
- Qu, X
- Somberg, J C
- Breithardt, G
- Oberti, C
- Funke, H
Producer: 19971204
In:
Nature genetics vol. 17
Availability: No items available.
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408297.
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408298.
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408299.
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Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB Group. [electronic resource] by
- Bennett, S T
- Wilson, A J
- Esposito, L
- Bouzekri, N
- Undlien, D E
- Cucca, F
- Nisticò, L
- Buzzetti, R
- Bosi, E
- Pociot, F
- Nerup, J
- Cambon-Thomsen, A
- Pugliese, A
- Shield, J P
- McKinney, P A
- Bain, S C
- Polychronakos, C
- Todd, J A
Producer: 19971204
In:
Nature genetics vol. 17
Availability: No items available.
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408300.
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