Wolf–Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16 Marcella ZollinoRosetta LecceGiovanni Neri Original Investigation 04 August 2007 Pages: 423 - 430
Tracing genetic history of modern humans using X-chromosome lineages Vania YotovaJean-François LefebvreDamian Labuda Original Investigation 07 August 2007 Pages: 431 - 443
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3 Quratul AinSabiha NazliSheikh Riazuddin Original Investigation 10 August 2007 Pages: 445 - 450
Genotype–phenotype correlations for SLC26A4-related deafness Hela AzaiezTao YangRichard J. H. Smith Original Investigation 10 August 2007 Pages: 451 - 457
High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndrome Katsunori FujiiShumpei IshikawaToshiyuki Miyashita Original Investigation 17 August 2007 Pages: 459 - 466
Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis Aurore CarréMireille CastanetMichel Polak Original Investigation 24 August 2007 Pages: 467 - 476
A most distant intergeneric hybrid offspring (Larcon) of lesser apes, Nomascus leucogenys and Hylobates lar Hirohisa HiraiYuriko HiraiYoko Kirihara Original Investigation 24 August 2007 Pages: 477 - 483
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. WalstonM. Daniele FallinAlex Reiner Original Investigation 13 September 2007 Pages: 485 - 494
Methods to impute missing genotypes for population data Zhaoxia YuDaniel J. Schaid Original Investigation 13 September 2007 Pages: 495 - 504
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-MaarriTim BeckerJohannes Oldenburg Original Investigation 13 September 2007 Pages: 505 - 514
RAAS gene polymorphisms influence progression of pediatric hypertrophic cardiomyopathy Beth D. KaufmanScott AuerbachSeema Mital Original Investigation 13 September 2007 Pages: 515 - 523
One-carbon metabolism gene polymorphisms and risk of non-Hodgkin lymphoma in Australia Kyoung-Mu LeeQing LanBruce K. Armstrong Original Investigation 21 September 2007 Pages: 525 - 533
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. RaiS. SharmaR. N. K. Bamezai Short Report 14 August 2007 Pages: 535 - 540
The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient Patricia Marques PereiraDelphine HeronAndré Hanauer Short Report 24 August 2007 Pages: 541 - 543
Barbara Migeon: Females are mosaics: X inactivation and sex differences in disease William Reardon Book Review 09 August 2007 Pages: 561 - 562
Imprinting detection by extending a regression-based QTL analysis method Olga Y. GorlovaLei LeiChristopher I. Amos Erratum 06 September 2007 Pages: 563 - 563
