1. Wolf–Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16

   • Marcella Zollino
   • Rosetta Lecce
   • Giovanni Neri

   Original Investigation 04 August 2007 Pages: 423 - 430

   

2. Tracing genetic history of modern humans using X-chromosome lineages

   • Vania Yotova
   • Jean-François Lefebvre
   • Damian Labuda

   Original Investigation 07 August 2007 Pages: 431 - 443

   

3. The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3

   • Quratul Ain
   • Sabiha Nazli
   • Sheikh Riazuddin

   Original Investigation 10 August 2007 Pages: 445 - 450

   

4. Genotype–phenotype correlations for SLC26A4-related deafness

   • Hela Azaiez
   • Tao Yang
   • Richard J. H. Smith

   Original Investigation 10 August 2007 Pages: 451 - 457

   

5. High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndrome

   • Katsunori Fujii
   • Shumpei Ishikawa
   • Toshiyuki Miyashita

   Original Investigation 17 August 2007 Pages: 459 - 466

   

6. Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis

   • Aurore Carré
   • Mireille Castanet
   • Michel Polak

   Original Investigation 24 August 2007 Pages: 467 - 476

   

7. A most distant intergeneric hybrid offspring (Larcon) of lesser apes, Nomascus leucogenys and Hylobates lar

   • Hirohisa Hirai
   • Yuriko Hirai
   • Yoko Kirihara

   Original Investigation 24 August 2007 Pages: 477 - 483

   

8. IL-6 gene variation is associated with IL-6 and C-reactive protein levels but not cardiovascular outcomes in the Cardiovascular Health Study

   • Jeremy D. Walston
   • M. Daniele Fallin
   • Alex Reiner

   Original Investigation 13 September 2007 Pages: 485 - 494

   

9. Methods to impute missing genotypes for population data

   • Zhaoxia Yu
   • Daniel J. Schaid

   Original Investigation 13 September 2007 Pages: 495 - 504

   

10. Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in males

    • Osman El-Maarri
    • Tim Becker
    • Johannes Oldenburg

    Original Investigation 13 September 2007 Pages: 505 - 514

    

11. RAAS gene polymorphisms influence progression of pediatric hypertrophic cardiomyopathy

    • Beth D. Kaufman
    • Scott Auerbach
    • Seema Mital

    Original Investigation 13 September 2007 Pages: 515 - 523

    

12. One-carbon metabolism gene polymorphisms and risk of non-Hodgkin lymphoma in Australia

    • Kyoung-Mu Lee
    • Qing Lan
    • Bruce K. Armstrong

    Original Investigation 21 September 2007 Pages: 525 - 533

    

13. Interaction between the UCP2–866G/A, mtDNA 10398G/A and PGC1α p.Thr394Thr and p.Gly482Ser polymorphisms in type 2 diabetes susceptibility in North Indian population

    • E. Rai
    • S. Sharma
    • R. N. K. Bamezai

    Short Report 14 August 2007 Pages: 535 - 540

14. The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient

    • Patricia Marques Pereira
    • Delphine Heron
    • André Hanauer

    Short Report 24 August 2007 Pages: 541 - 543

    

15. Novel human pathological mutations

    Human Gene Mutations 13 September 2007 Pages: 545 - 559

16. Barbara Migeon: Females are mosaics: X inactivation and sex differences in disease

    • William Reardon

    Book Review 09 August 2007 Pages: 561 - 562

17. Imprinting detection by extending a regression-based QTL analysis method

    • Olga Y. Gorlova
    • Lei Lei
    • Christopher I. Amos

    Erratum 06 September 2007 Pages: 563 - 563