Results
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3821.
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3822.
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3823.
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3824.
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3825.
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3826.
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3827.
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Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. [electronic resource] by
- David, G
- Abbas, N
- Stevanin, G
- Dürr, A
- Yvert, G
- Cancel, G
- Weber, C
- Imbert, G
- Saudou, F
- Antoniou, E
- Drabkin, H
- Gemmill, R
- Giunti, P
- Benomar, A
- Wood, N
- Ruberg, M
- Agid, Y
- Mandel, J L
- Brice, A
Producer: 19971002
In:
Nature genetics vol. 17
Availability: No items available.
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3828.
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hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats with schizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21. [electronic resource] by
- Dror, V
- Shamir, E
- Ghanshani, S
- Kimhi, R
- Swartz, M
- Barak, Y
- Weizman, R
- Avivi, L
- Litmanovitch, T
- Fantino, E
- Kalman, K
- Jones, E G
- Chandy, K G
- Gargus, J J
- Gutman, G A
- Navon, R
Producer: 19990913
In:
Molecular psychiatry vol. 4
Availability: No items available.
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3829.
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3830.
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3831.
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3832.
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A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats. [electronic resource] by
- Chung, Boi-Dinh
- Kayserili, Hülya
- Ai, Minrong
- Freudenberg, Jan
- Uzümcü, Abdullah
- Uyguner, Oya
- Bartels, Cynthia F
- Höning, Stefan
- Ramirez, Alfredo
- Hanisch, Franz-Georg
- Nürnberg, Gudrun
- Nürnberg, Peter
- Warman, Matthew L
- Wollnik, Bernd
- Kubisch, Christian
- Netzer, Christian
Producer: 20090706
In:
Human mutation vol. 30
Availability: No items available.
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3833.
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3834.
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3835.
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3836.
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Association between anorexia nervosa and the hsKCa3 gene: a family-based and case control study. [electronic resource] by
- Koronyo-Hamaoui, M
- Danziger, Y
- Frisch, A
- Stein, D
- Leor, S
- Laufer, N
- Carel, C
- Fennig, S
- Minoumi, M
- Apter, A
- Goldman, B
- Barkai, G
- Weizman, A
- Gak, E
Producer: 20020419
In:
Molecular psychiatry vol. 7
Availability: No items available.
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3837.
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3838.
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3839.
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3840.
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