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Npj genomic medicine, 2017-05, Vol.2 (1), p.16-9, Article 16
2017
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PLoS genetics, 2007-06, Vol.3 (6), p.e108
- van de Leemput, Joyce
- Chandran, Jayanth
- Knight, Melanie A
- Holtzclaw, Lynne A
- Scholz, Sonja
- Cookson, Mark R
- Houlden, Henry
- Gwinn-Hardy, Katrina
- Fung, Hon-Chung
- Lin, Xian
- Hernandez, Dena
- Simon-Sanchez, Javier
- Wood, Nick W
- Giunti, Paola
- Rafferty, Ian
- Hardy, John
- Storey, Elsdon
- Gardner, R J McKinlay
- Forrest, Susan M
- Fisher, Elizabeth M C
- Russell, James T
- Cai, Huaibin
- Singleton, Andrew B
- Orr, Harry
2007
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Npj genomic medicine, 2017-10, Vol.2 (1), p.31-1, Article 31
2017
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BMC medical genetics, 2008-03, Vol.9 (1), p.18-18, Article 18
2008
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Journal of Medical Genetics, 2000-01, Vol.37 (1), p.1-8
2000
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Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20
2004
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Human molecular genetics, 2008-12, Vol.17 (24), p.3847-3853
2008
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Human mutation, 2005-10, Vol.26 (4), p.384-389
2005
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Neurobiology of disease, 2003-07, Vol.13 (2), p.147-157
2003
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Genomics (San Diego, Calif.), 2002-04, Vol.79 (4), p.553-559
2002
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Journal of medical genetics, 2007-04, Vol.44 (4), p.e75-e75
2007
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Journal of investigative dermatology, 2004-12, Vol.123 (6), p.1070-1072
2004
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European journal of human genetics : EJHG, 2002-10, Vol.10 (10), p.623-630
2002
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Cerebellum (London, England), 2005-01, Vol.4 (1), p.47-50
2005
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European journal of human genetics : EJHG, 2003-10, Vol.11 (10), p.779-783
2003
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American journal of medical genetics, 2002-07, Vol.110 (4), p.397-399
2002
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Genome biology, 2011-08, Vol.12 (8), p.R81-R81
- Renfree, Marilyn B
- Papenfuss, Anthony T
- Deakin, Janine E
- Lindsay, James
- Heider, Thomas
- Belov, Katherine
- Rens, Willem
- Waters, Paul D
- Pharo, Elizabeth A
- Shaw, Geoff
- Wong, Emily S W
- Lefèvre, Christophe M
- Nicholas, Kevin R
- Kuroki, Yoko
- Wakefield, Matthew J
- Wang, Chenwei
- Ferguson-Smith, Malcolm
- Nicholas, Frank W
- Hickford, Danielle
- Yu, Hongshi
- Short, Kirsty R
- Siddle, Hannah V
- Frankenberg, Stephen R
- Chew, Keng Yih
- Menzies, Brandon R
- Stringer, Jessica M
- Suzuki, Shunsuke
- Hore, Timothy A
- Delbridge, Margaret L
- Patel, Hardip R
- Mohammadi, Amir
- Schneider, Nanette Y
- Hu, Yanqiu
- O'Hara, William
- Al Nadaf, Shafagh
- Wu, Chen
- Feng, Zhi-Ping
- Cocks, Benjamin G
- Wang, Jianghui
- Flicek, Paul
- Searle, Stephen M J
- Fairley, Susan
- Beal, Kathryn
- Herrero, Javier
- Carone, Dawn M
- Suzuki, Yutaka
- Sugano, Sumio
- Toyoda, Atsushi
- Sakaki, Yoshiyuki
- Kondo, Shinji
- Nishida, Yuichiro
- Tatsumoto, Shoji
- Mandiou, Ion
- Hsu, Arthur
- McColl, Kaighin A
- Lansdell, Benjamin
- Weinstock, George
- Kuczek, Elizabeth
- McGrath, Annette
- Wilson, Peter
- Men, Artem
- Hazar-Rethinam, Mehlika
- Hall, Allison
- Davis, John
- Wood, David
- Williams, Sarah
- Muzny, Donna M
- Jhangiani, Shalini N
- Lewis, Lora R
- Morgan, Margaret B
- Okwuonu, Geoffrey O
- Ruiz, San Juana
- Nazareth, Lynne
- Cree, Andrew
- Fowler, Gerald
- Kovar, Christie L
- Dinh, Huyen H
- Joshi, Vandita
- Jing, Chyn
- Lara, Fremiet
- Thornton, Rebecca
- Chen, Lei
- Deng, Jixin
- Liu, Yue
- Shen, Joshua Y
- Song, Xing-Zhi
- Edson, Janette
- Troon, Carmen
- Thomas, Daniel
- Stephens, Amber
- Yapa, Lankesha
- Levchenko, Tanya
- Gibbs, Richard A
- Cooper, Desmond W
- Speed, Terence P
- Fujiyama, Asao
- Graves, Jennifer A M
- O'Neill, Rachel J
- Pask, Andrew J
- Forrest, Susan M
2011
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The journal of gene medicine, 2001-01, Vol.3 (1), p.72-81
2001
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American journal of medical genetics, 1999-11, Vol.87 (2), p.168-174
1999
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The Journal of investigative dermatology symposium proceedings, 2003-06, Vol.8 (1), p.121-125
2003
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Human mutation, 2000-10, Vol.16 (4), p.374-374
2000
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Movement disorders, 2001-09, Vol.16 (5), p.938-939
2001
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American journal of medical genetics, 2000-12, Vol.95 (4), p.351-358
2000
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Pediatric research, 1999-04, Vol.45 (4), p.474-481
1999
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Journal of allergy and clinical immunology, 2002-01, Vol.109 (1), p.176-178
2002
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