Results
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1701.
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Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas. [electronic resource] by
- Sarrión, P
- Sangorrin, A
- Urreizti, R
- Delgado, A
- Artuch, R
- Martorell, L
- Armstrong, J
- Anton, J
- Torner, F
- Vilaseca, M A
- Nevado, J
- Lapunzina, P
- Asteggiano, C G
- Balcells, S
- Grinberg, D
Producer: 20130816
In:
Scientific reports vol. 3
Availability: No items available.
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1702.
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Role of microsatellite instability-low as a diagnostic biomarker of Lynch syndrome in colorectal cancer. [electronic resource] by
- Vilar, Eduardo
- Mork, Maureen E
- Cuddy, Amanda
- Borras, Ester
- Bannon, Sarah A
- Taggart, Melissa W
- Ying, Jun
- Broaddus, Russell R
- Luthra, Rajyalakshmi
- Rodriguez-Bigas, Miguel A
- Lynch, Patrick M
- You, Yi-Qian Nancy
Producer: 20150224
In:
Cancer genetics vol. 207
Availability: No items available.
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1703.
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Whole genome sequencing of Mycobacterium tuberculosis reveals slow growth and low mutation rates during latent infections in humans. [electronic resource] by
- Colangeli, Roberto
- Arcus, Vic L
- Cursons, Ray T
- Ruthe, Ali
- Karalus, Noel
- Coley, Kathy
- Manning, Shannon D
- Kim, Soyeon
- Marchiano, Emily
- Alland, David
Producer: 20150529
In:
PloS one vol. 9
Availability: No items available.
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1704.
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1705.
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1706.
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1707.
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Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort. [electronic resource] by
- Landoulsi, Zied
- Benromdhan, Sawssan
- Ben Djebara, Mouna
- Damak, Mariem
- Dallali, Hamza
- Kefi, Rym
- Abdelhak, Sonia
- Gargouri-Berrechid, Amina
- Mhiri, Chokri
- Gouider, Riadh
Producer: 20170724
In:
BMC medical genetics vol. 18
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1708.
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1709.
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1710.
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Extensive Variation in the Mutation Rate Between and Within Human Genes Associated with Mendelian Disease. [electronic resource] by
- Smith, Thomas
- Ho, Gladys
- Christodoulou, John
- Price, Elizabeth Ann
- Onadim, Zerrin
- Gauthier-Villars, Marion
- Dehainault, Catherine
- Houdayer, Claude
- Parfait, Beatrice
- van Minkelen, Rick
- Lohman, Dietmar
- Eyre-Walker, Adam
Producer: 20161228
In:
Human mutation vol. 37
Availability: No items available.
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1711.
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Whole-Exome Sequencing Reveals Frequent Mutations in Chromatin Remodeling Genes in Mammary and Extramammary Paget's Diseases. [electronic resource] by
- Zhang, Guohong
- Zhou, Songxia
- Zhong, Weixiang
- Hong, Liangli
- Wang, Yuanyuan
- Lu, Shanming
- Pan, Jiankai
- Huang, Yuansheng
- Su, Mingwan
- Crawford, Richard
- Zhou, Youwen
- Mai, Ruiqin
Producer: 20200402
In:
The Journal of investigative dermatology vol. 139
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1714.
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Targeted deep sequencing from multiple sources demonstrates increased NOTCH1 alterations in lung cancer patient plasma. [electronic resource] by
- Liao, Yuwei
- Ma, Zhaokui
- Zhang, Yu
- Li, Dan
- Lv, Dekang
- Chen, Zhisheng
- Li, Peiying
- Ai-Dherasi, Aisha
- Zheng, Feng
- Tian, Jichao
- Zou, Kun
- Wang, Yue
- Wang, Dongxia
- Cordova, Miguel
- Zhou, Huan
- Li, Xiuhua
- Liu, Dan
- Yu, Ruofei
- Zhang, Qingzheng
- Zhang, Xiaolong
- Zhang, Jian
- Zhang, Xuehong
- Zhang, Xia
- Li, Yulong
- Shao, Yanyan
- Song, Luyao
- Liu, Ruimei
- Wang, Yichen
- Sufiyan, Sufiyan
- Liu, Quentin
- Owen, Gareth I
- Li, Zhiguang
- Chen, Jun
Producer: 20200821
In:
Cancer medicine vol. 8
Availability: No items available.
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