Results
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26621.
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26622.
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26623.
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Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly). [electronic resource] by
- Hoffmann, Katrin
- Dreger, Christine K
- Olins, Ada L
- Olins, Donald E
- Shultz, Leonard D
- Lucke, Barbara
- Karl, Hartmut
- Kaps, Reinhard
- Müller, Dietmar
- Vayá, Amparo
- Aznar, Justo
- Ware, Russell E
- Sotelo Cruz, Norberto
- Lindner, Tom H
- Herrmann, Harald
- Reis, André
- Sperling, Karl
Producer: 20020906
In:
Nature genetics vol. 31
Availability: No items available.
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26624.
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26625.
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26626.
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26627.
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26628.
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26629.
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A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q. [electronic resource] by
- Bakker, S C
- van der Meulen, E M
- Buitelaar, J K
- Sandkuijl, L A
- Pauls, D L
- Monsuur, A J
- van 't Slot, R
- Minderaa, R B
- Gunning, W B
- Pearson, P L
- Sinke, R J
Producer: 20030701
In:
American journal of human genetics vol. 72
Availability: No items available.
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26630.
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A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families. [electronic resource] by
- Yakobson, Emanuel
- Eisenberg, Shlomit
- Isacson, Ruth
- Halle, David
- Levy-Lahad, Efrat
- Catane, Raphael
- Safro, Mark
- Sobolev, Vladimir
- Huot, Thomas
- Peters, Gordon
- Ruiz, Anna
- Malvehy, Josep
- Puig, Suzana
- Chompret, Agnes
- Avril, Marie-Fracoise
- Shafir, Raphael
- Peretz, Hava
- Bressac-de Paillerets, Brigitte
Producer: 20031121
In:
European journal of human genetics : EJHG vol. 11
Availability: No items available.
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26631.
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26632.
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26633.
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26634.
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26635.
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26636.
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26637.
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26638.
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26639.
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26640.
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