Genetic polymorphisms in transforming growth factor beta-1 (TGFB1) and childhood asthma and atopy Huiling LiIsabelle RomieuStephanie J. London Original Investigation 28 February 2007 Pages: 529 - 538
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 FroyenMarijke BautersGillian Turner Original Investigation 28 February 2007 Pages: 539 - 547
Testing for association based on excess allele sharing in a sample of related cases and controls Lambertus KleiKathyrn Roeder Original Investigation 07 March 2007 Pages: 549 - 557
A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36 Sumana GopinathIan P. BlairGarth A. Nicholson Original Investigation 13 March 2007 Pages: 559 - 564
Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA Study Alexander P. ReinerChristopher S. CarlsonDeborah A. Nickerson Original Investigation 14 March 2007 Pages: 565 - 575
An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP) C. Charles GuSteven C. HuntD. C. Rao Original Investigation 20 March 2007 Pages: 577 - 590
Molecular diagnostics of Meckel–Gruber syndrome highlights phenotypic differences between MKS1 and MKS3 Mark B. ConsugarVickie J. KublyPeter C. Harris Original Investigation 22 March 2007 Pages: 591 - 599
Association of ALOX5AP with ischemic stroke: a population-based case-control study Ritesh KaushalProdipto PalDaniel Woo Original Investigation 27 March 2007 Pages: 601 - 607
PGC-1α Thr394Thr and Gly482Ser variants are significantly associated with T2DM in two North Indian populations: a replicate case-control study Audesh BhatAnil KoulR. N. K. Bamezai Original Investigation 28 March 2007 Pages: 609 - 614
Genetic admixture, adipocytokines, and adiposity in Black Americans: the Health, Aging, and Body Composition study Christina L. Wassel FyrAlka M. Kanayafor the Health, Aging, Body Composition Study Original Investigation 28 March 2007 Pages: 615 - 624
A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese family Yoshinari MiyamotoTatsuo MatsudaShiro Ikegawa Original Investigation 30 March 2007 Pages: 625 - 629
A strong association between human earwax-type and apocrine colostrum secretion from the mammary gland Kiyonori MiuraKoh-ichiro YoshiuraHideaki Masuzaki Short Report 30 March 2007 Pages: 631 - 633
The P239S palladin variant does not account for a significant fraction of hereditary or early onset pancreas cancer George ZogopoulousHeidi RothenmundSteven Gallinger Short Report 06 April 2007 Pages: 635 - 637
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
Kenneth Lyons Jones (ed): Smith’s recognizable patterns of human malformation I. K. Temple Book Review 06 February 2007 Pages: 641 - 642
Anthony H. Futerman, Ari Zimran: Gaucher Disease Ed Wraith Book Review 16 February 2007 Pages: 643 - 644
Genetic markers for glutamic acid decarboxylase do not predict insulin-dependent diabetes mellitus in pairs of affected siblings Tina RambrandFlemming PociotThe Danish Study Group of Diabetes in Childhood Erratum 07 February 2007 Pages: 653 - 653
