1. Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC

   • Amanda J. DuBose
   • Karen A. Johnstone
   • James L. Resnick

   ORIGINAL ARTICLE 06 November 2009 Pages: 145 - 151

   

2. The C15orf2 gene in the Prader–Willi syndrome region is subject to genomic imprinting and positive selection

   • Michaela Wawrzik
   • Unga Arifa Unmehopa
   • Bernhard Horsthemke

   ORIGINAL ARTICLE 19 December 2009 Pages: 153 - 161

   

3. Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene

   • Gabriele Dekomien
   • Conni Vollrath
   • Jörg T. Epplen

   ORIGINAL ARTICLE 24 September 2009 Pages: 163 - 174

   

4. Congenital bovine spinal dysmyelination is caused by a missense mutation in the SPAST gene

   • Bo Thomsen
   • Peter H. Nissen
   • Christian Bendixen

   ORIGINAL ARTICLE Open access 28 August 2009 Pages: 175 - 183

   

5. A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse

   • Sarah E. Lloyd
   • Emma G. Maytham
   • John Collinge

   ORIGINAL ARTICLE Open access 01 October 2009 Pages: 185 - 191

   

6. Increased transcript diversity: novel splicing variants of Machado–Joseph Disease gene (ATXN3)

   • Conceição Bettencourt
   • Cristina Santos
   • Manuela Lima

   ORIGINAL ARTICLE 28 August 2009 Pages: 193 - 202

   

7. Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's disease

   • Anne S. Soehn
   • Thomas Franck
   • Olaf Riess

   ORIGINAL ARTICLE 03 September 2009 Pages: 203 - 215

   

8. Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis

   • Janine Kirby
   • Emily F. Goodall
   • Pamela J. Shaw

   ORIGINAL ARTICLE 17 September 2009 Pages: 217 - 225

   

9. Intratumoral patterns of clonal evolution in gliomas

   • Ana Luísa Vital
   • Maria Dolores Tabernero
   • Alberto Orfao

   ORIGINAL ARTICLE 17 September 2009 Pages: 227 - 239

   

10. Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant

    • Nadia Bahi-Buisson
    • Juliette Nectoux
    • Thierry Bienvenu

    ORIGINAL ARTICLE 06 October 2009 Pages: 241 - 249

    

11. A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation

    • Ginevra Zanni
    • Hilde van Esch
    • Jamel Chelly

    SHORT COMMUNICATION 01 October 2009 Pages: 251 - 255

    

12. Isolated eyelid closure myotonia in two families with sodium channel myotonia

    • B. C. Stunnenberg
    • H. B. Ginjaar
    • G. Drost

    SHORT COMMUNICATION Open access 30 October 2009 Pages: 257 - 260

    

13. Atypical, perhaps under-recognized? An unusual phenotype of Friedreich ataxia

    • Beate Diehl
    • Michael S. Lee
    • Marvin R. Natowicz

    SHORT COMMUNICATION 17 February 2010 Pages: 261 - 265

    

14. X-linked CMT: genes and gene loci in an Australian cohort

    • Megan Hwa Brewer
    • Rabia Chaudhry
    • Marina Kennerson

    LETTER TO THE EDITORS 05 March 2010 Pages: 267 - 269

    

15. Suggestive evidence on chromosomes 2 and 19 for HTR1A-independent linkage of genes to major depression

    • Victor Abkevich
    • Chris D. Neff
    • David A. Katz

    LETTER 08 October 2009 Pages: 271 - 272

    

16. Evidence against haploinsuffiency of human ataxin 10 as a cause of spinocerebellar ataxia type 10

    • Boris Keren
    • Aurélia Jacquette
    • Delphine Héron

    LETTER 20 November 2009 Pages: 273 - 274