1. Genetic polymorphisms in transforming growth factor beta-1 (TGFB1) and childhood asthma and atopy

   • Huiling Li
   • Isabelle Romieu
   • Stephanie J. London

   Original Investigation 28 February 2007 Pages: 529 - 538

2. Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region

   • Guy Froyen
   • Marijke Bauters
   • Gillian Turner

   Original Investigation 28 February 2007 Pages: 539 - 547

   

3. Testing for association based on excess allele sharing in a sample of related cases and controls

   • Lambertus Klei
   • Kathyrn Roeder

   Original Investigation 07 March 2007 Pages: 549 - 557

   

4. A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36

   • Sumana Gopinath
   • Ian P. Blair
   • Garth A. Nicholson

   Original Investigation 13 March 2007 Pages: 559 - 564

   

5. Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA Study

   • Alexander P. Reiner
   • Christopher S. Carlson
   • Deborah A. Nickerson

   Original Investigation 14 March 2007 Pages: 565 - 575

6. An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP)

   • C. Charles Gu
   • Steven C. Hunt
   • D. C. Rao

   Original Investigation 20 March 2007 Pages: 577 - 590

   

7. Molecular diagnostics of Meckel–Gruber syndrome highlights phenotypic differences between MKS1 and MKS3

   • Mark B. Consugar
   • Vickie J. Kubly
   • Peter C. Harris

   Original Investigation 22 March 2007 Pages: 591 - 599

   

8. Association of ALOX5AP with ischemic stroke: a population-based case-control study

   • Ritesh Kaushal
   • Prodipto Pal
   • Daniel Woo

   Original Investigation 27 March 2007 Pages: 601 - 607

   

9. PGC-1α Thr394Thr and Gly482Ser variants are significantly associated with T2DM in two North Indian populations: a replicate case-control study

   • Audesh Bhat
   • Anil Koul
   • R. N. K. Bamezai

   Original Investigation 28 March 2007 Pages: 609 - 614

10. Genetic admixture, adipocytokines, and adiposity in Black Americans: the Health, Aging, and Body Composition study

    • Christina L. Wassel Fyr
    • Alka M. Kanaya
    • for the Health, Aging, Body Composition Study

    Original Investigation 28 March 2007 Pages: 615 - 624

11. A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese family

    • Yoshinari Miyamoto
    • Tatsuo Matsuda
    • Shiro Ikegawa

    Original Investigation 30 March 2007 Pages: 625 - 629

    

12. A strong association between human earwax-type and apocrine colostrum secretion from the mammary gland

    • Kiyonori Miura
    • Koh-ichiro Yoshiura
    • Hideaki Masuzaki

    Short Report 30 March 2007 Pages: 631 - 633

    

13. The P239S palladin variant does not account for a significant fraction of hereditary or early onset pancreas cancer

    • George Zogopoulous
    • Heidi Rothenmund
    • Steven Gallinger

    Short Report 06 April 2007 Pages: 635 - 637

14. J. R. Lupski and P.T. Stankiewicz: Genomic disorders: the genomic basis of disease

    • Charles Shaw-Smith

    Book Review 14 February 2007 Pages: 639 - 640

15. Kenneth Lyons Jones (ed): Smith’s recognizable patterns of human malformation

    • I. K. Temple

    Book Review 06 February 2007 Pages: 641 - 642

16. Anthony H. Futerman, Ari Zimran: Gaucher Disease

    • Ed Wraith

    Book Review 16 February 2007 Pages: 643 - 644

17. Novel human pathological mutations

    Human Gene Mutations 13 April 2007 Pages: 645 - 652

18. Genetic markers for glutamic acid decarboxylase do not predict insulin-dependent diabetes mellitus in pairs of affected siblings

    • Tina Rambrand
    • Flemming Pociot
    • The Danish Study Group of Diabetes in Childhood

    Erratum 07 February 2007 Pages: 653 - 653