Results
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81.
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82.
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83.
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84.
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85.
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86.
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87.
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Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2. [electronic resource] by
- Vincent, Lisa M
- Gilbert, Fred
- DiPace, Jennifer I
- Ciccone, Carla
- Markello, Thomas C
- Jeong, Andrew
- Dorward, Heidi
- Westbroek, Wendy
- Gahl, William A
- Bussel, James B
- Huizing, Marjan
Producer: 20110124
In:
Molecular genetics and metabolism vol. 101
Availability: No items available.
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88.
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Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility. [electronic resource] by
- Chen, Hongyan
- Chen, Gong
- Li, Gang
- Zhang, Shuo
- Chen, Haitao
- Chen, Yuanyuan
- Duggan, Dave
- Hu, Zhibin
- Chen, Juxing
- Zhao, Yingjie
- Zhao, Yao
- Huang, Huiling
- Zheng, S Lilly
- Trent, Jeffrey M
- Yu, Long
- Jiang, Deke
- Mo, Zengnan
- Wang, Hongwei
- Mou, Yonggao
- Jiang, Tao
- Mao, Ying
- Xu, Jianfeng
- Lu, Daru
Producer: 20200123
In:
International journal of cancer vol. 145
Availability: No items available.
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89.
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90.
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91.
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92.
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93.
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94.
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95.
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96.
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97.
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98.
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99.
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Evidence that Griscelli syndrome with neurological involvement is caused by mutations in RAB27A, not MYO5A. [electronic resource] by
- Anikster, Yair
- Huizing, Marjan
- Anderson, Paul D
- Fitzpatrick, Diana L
- Klar, Aharon
- Gross-Kieselstein, Eva
- Berkun, Yackov
- Shazberg, Gila
- Gahl, William A
- Hurvitz, Haggit
Producer: 20020820
In:
American journal of human genetics vol. 71
Availability: No items available.
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100.
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