Excavating Y-chromosome haplotype strata in Anatolia Cengiz CinnioğluRoy KingPeter A. Underhill Original Investigation 29 October 2003 Pages: 127 - 148
Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy Marco SifringerBirgit UhlenbergAstrid Speer Original Investigation 05 November 2003 Pages: 149 - 156
A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma Malcolm N. BlumenthalCarl D. LangefeldStephen S. Rich Original Investigation 25 October 2003 Pages: 157 - 164
A comparison of the mutation spectra of Menkes disease and Wilson disease Gloria HsiDiane W. Cox Original Investigation 25 October 2003 Pages: 165 - 172
Molecular and evolutionary analysis of the growth-controlling region on the human Y chromosome Stefan KirschBirgit WeissGudrun Rappold Original Investigation 25 October 2003 Pages: 173 - 181
The thymidylate synthase tandem repeat polymorphism is not associated with homocysteine concentrations in healthy young subjects Karen S. BrownLeo A. J. KluijtmansAlexander S. Whitehead Original Investigation 25 October 2003 Pages: 182 - 185
The impact of factor XIIIa V34L polymorphism on plasma factor XIII activity in the Chinese and Asian Indians from Singapore Chew-Kiat HengSuman LalM. Ilyas Kamboh Original Investigation 31 October 2003 Pages: 186 - 191
A deletion mutation in the βA1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family Yanhua QiHongyan JiaYing Li Original Investigation 04 November 2003 Pages: 192 - 197
Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements Blake C. BallifKeiko WakuiLisa G. Shaffer Original Investigation 25 October 2003 Pages: 198 - 206
Inherited variants in MYH are unlikely to contribute to the risk of lung carcinoma Nada Al-TassanTim EisenRichard S. Houlston Short Report 25 October 2003 Pages: 207 - 210
Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation Tero Ylisaukko-ojaKarola RehnströmIrma Järvelä Short Report 04 November 2003 Pages: 211 - 213
On the applicability of a haplotype map to un-assayed populations Itsik Pe’erJacques S. Beckmann Letter to the Editors 25 October 2003 Pages: 214 - 217
David Bainbridge (Editor), The X in sex: how the X chromosome controls our lives Andrew P. Read Book Review 06 November 2003 Pages: 218 - 218
Hugh Markus (Editor) Report on stroke genetics Steve E. Humphries Book Review 08 November 2003 Pages: 219 - 219
Rowena Spencer (Editor) Conjoined twins. Developmental malformations and clinical implications Robert A. Wheeler Book Review 25 October 2003 Pages: 220 - 220
