Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC Amanda J. DuBoseKaren A. JohnstoneJames L. Resnick ORIGINAL ARTICLE 06 November 2009 Pages: 145 - 151
The C15orf2 gene in the Prader–Willi syndrome region is subject to genomic imprinting and positive selection Michaela WawrzikUnga Arifa UnmehopaBernhard Horsthemke ORIGINAL ARTICLE 19 December 2009 Pages: 153 - 161
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene Gabriele DekomienConni VollrathJörg T. Epplen ORIGINAL ARTICLE 24 September 2009 Pages: 163 - 174
Congenital bovine spinal dysmyelination is caused by a missense mutation in the SPAST gene Bo ThomsenPeter H. NissenChristian Bendixen ORIGINAL ARTICLE Open access 28 August 2009 Pages: 175 - 183
A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse Sarah E. LloydEmma G. MaythamJohn Collinge ORIGINAL ARTICLE Open access 01 October 2009 Pages: 185 - 191
Increased transcript diversity: novel splicing variants of Machado–Joseph Disease gene (ATXN3) Conceição BettencourtCristina SantosManuela Lima ORIGINAL ARTICLE 28 August 2009 Pages: 193 - 202
Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's disease Anne S. SoehnThomas FranckOlaf Riess ORIGINAL ARTICLE 03 September 2009 Pages: 203 - 215
Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis Janine KirbyEmily F. GoodallPamela J. Shaw ORIGINAL ARTICLE 17 September 2009 Pages: 217 - 225
Intratumoral patterns of clonal evolution in gliomas Ana Luísa VitalMaria Dolores TaberneroAlberto Orfao ORIGINAL ARTICLE 17 September 2009 Pages: 227 - 239
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant Nadia Bahi-BuissonJuliette NectouxThierry Bienvenu ORIGINAL ARTICLE 06 October 2009 Pages: 241 - 249
A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation Ginevra ZanniHilde van EschJamel Chelly SHORT COMMUNICATION 01 October 2009 Pages: 251 - 255
Isolated eyelid closure myotonia in two families with sodium channel myotonia B. C. StunnenbergH. B. GinjaarG. Drost SHORT COMMUNICATION Open access 30 October 2009 Pages: 257 - 260
Atypical, perhaps under-recognized? An unusual phenotype of Friedreich ataxia Beate DiehlMichael S. LeeMarvin R. Natowicz SHORT COMMUNICATION 17 February 2010 Pages: 261 - 265
X-linked CMT: genes and gene loci in an Australian cohort Megan Hwa BrewerRabia ChaudhryMarina Kennerson LETTER TO THE EDITORS 05 March 2010 Pages: 267 - 269
Suggestive evidence on chromosomes 2 and 19 for HTR1A-independent linkage of genes to major depression Victor AbkevichChris D. NeffDavid A. Katz LETTER 08 October 2009 Pages: 271 - 272
Evidence against haploinsuffiency of human ataxin 10 as a cause of spinocerebellar ataxia type 10 Boris KerenAurélia JacquetteDelphine Héron LETTER 20 November 2009 Pages: 273 - 274