Update on the genetics of migraine Miguel EstevezKathy L. Gardner Review Article 18 November 2003 Pages: 225 - 235
Analysis of heat-shock protein 70 gene polymorphisms and the risk of Parkinson’s disease Yih-Ru WuCheng-Kuang WangGuey-Jen Lee-Chen Original Investigation 06 November 2003 Pages: 236 - 241
A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia Dolrudee JumlongrasJenn-Yih LinBjorn R. Olsen Original Investigation 19 December 2003 Pages: 242 - 249
Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm James M. FarnhamNicola J. CampLisa A. Cannon-Albright Original Investigation 06 November 2003 Pages: 250 - 255
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias Laurent GouyaHervé PuyJean-Charles Deybach Original Investigation 11 December 2003 Pages: 256 - 262
Mexican American ancestry-informative markers: examination of population structure and marker characteristics in European Americans, Mexican Americans, Amerindians and Asians Heather E. Collins-SchrammBill ChimaMichael F. Seldin Original Investigation 20 November 2003 Pages: 263 - 271
Haplotype mapping of the bronchiolitis susceptibility locus near IL8 Jeremy HullKate RowlandsDominic P. Kwiatkowski Original Investigation 06 November 2003 Pages: 272 - 279
Apolipoprotein B-100 XbaI gene polymorphism in gallbladder cancer Mahendra Kumar SinghUdai Bhan PandeyBalraj Mittal Original Investigation 14 November 2003 Pages: 280 - 283
Genetic and clinical mosaicism in a patient with neurofibromatosis type 1 Ina VandenbrouckeRemco van DoornLudwine Messiaen Original Investigation 06 November 2003 Pages: 284 - 290
Localized aggressive periodontitis is linked to human chromosome 1q25 Yefu LiLin XuThomas E. Van Dyke Original Investigation 12 December 2003 Pages: 291 - 297
Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28 Nadine GigarelNelly FrydmanPierre F. Ray Original Investigation 12 December 2003 Pages: 298 - 305
Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy Anna KaminskaSergei V. StrelkovLev G. Goldfarb Original Investigation 27 November 2003 Pages: 306 - 313
Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria Joaquim CaladoKarina SotoJosé Rueff Short Report 12 November 2003 Pages: 314 - 316
Bronya J.B. Keats, Arthur N. Popper, Richard R. Fay (Editors) Springer handbook of auditory research: genetics and auditory disorders Richard C. Trembath Book Review 11 December 2003 Pages: 317 - 317
Genetics and genomics of neurobehavioral disorders Randi J. Hagerman Book Review 11 December 2003 Pages: 318 - 319
G. Bates, P. Harper, L. Jones (eds): Huntington’s Disease, Third Edition Allan J. Tobin Book Review 09 December 2003 Pages: 320 - 321
Members of the CDY family have different expression patterns: CDY1 transcripts have the best correlation with complete spermatogenesis Sandra E. KleimanLeah YogevHaim Yavetz Erratum 12 December 2003 Pages: 322 - 322