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30721.
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30722.
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30723.
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Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n. [electronic resource] by
- Sato, Nozomu
- Amino, Takeshi
- Kobayashi, Kazuhiro
- Asakawa, Shuichi
- Ishiguro, Taro
- Tsunemi, Taiji
- Takahashi, Makoto
- Matsuura, Tohru
- Flanigan, Kevin M
- Iwasaki, Sawa
- Ishino, Fumitoshi
- Saito, Yuko
- Murayama, Shigeo
- Yoshida, Mari
- Hashizume, Yoshio
- Takahashi, Yuji
- Tsuji, Shoji
- Shimizu, Nobuyoshi
- Toda, Tatsushi
- Ishikawa, Kinya
- Mizusawa, Hidehiro
Producer: 20091222
In:
American journal of human genetics vol. 85
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30724.
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30725.
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Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family. [electronic resource] by
- Liu, Mugen
- Ke, Tie
- Wang, Zhaoxiang
- Yang, Qinbo
- Chang, Wei
- Jiang, Fagang
- Tang, Zhaohui
- Li, Hui
- Ren, Xiang
- Wang, Xu
- Wang, Tao
- Li, Qingchun
- Yang, Junguo
- Liu, Jingyu
- Wang, Qing Kenneth
Producer: 20060831
In:
Investigative ophthalmology & visual science vol. 47
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30726.
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30727.
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Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity. [electronic resource] by
- Mead, Simon
- Poulter, Mark
- Beck, Jon
- Webb, Thomas E F
- Campbell, Tracy A
- Linehan, Jacqueline M
- Desbruslais, Melanie
- Joiner, Susan
- Wadsworth, Jonathan D F
- King, Andrew
- Lantos, Peter
- Collinge, John
Producer: 20061004
In:
Brain : a journal of neurology vol. 129
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30728.
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30729.
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30730.
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New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes. [electronic resource] by
- Devos, David
- Vuillaume, Isabelle
- de Becdelievre, Alix
- de Martinville, Berengère
- Dhaenens, Claire-Marie
- Cuvellier, Jean-Christophe
- Cuisset, Jean-Marie
- Vallée, Louis
- Lemaitre, Marie-Pierre
- Bourteel, Hélène
- Hachulla, Eric
- Wallaert, Benoit
- Destée, Alain
- Defebvre, Luc
- Sablonnière, Bernard
Producer: 20070220
In:
Movement disorders : official journal of the Movement Disorder Society vol. 21
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30731.
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30732.
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30733.
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30734.
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30736.
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30737.
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30738.
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30739.
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TNFa-e microsatellite, HLA-DRB1 and -DQB1 alleles and haplotypes in Brazilian patients presenting recently diagnosed type 1 diabetes mellitus. [electronic resource] by
- Rassi, Diane M
- Wastowski, Isabela J
- Simões, Renata T
- Rodrigues, Sandra
- Deghaide, Neife N H S
- Mendes-Junior, Celso T
- Simões, Aguinaldo L
- Soares, C P
- Passos, Geraldo A S
- Donadi, Eduardo A
Producer: 20070110
In:
Annals of the New York Academy of Sciences vol. 1079
Availability: No items available.
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30740.
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