Investigation of the functional effect of monoamine oxidase polymorphisms in human brain J. BalciunieneL. EmilssonE. Jazin Original Investigation 07 December 2001 Pages: 1 - 7
Familial idiopathic basal ganglia calcification (Fahr's disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q Henry BrodatyPhilip MitchellPeter R. Schofield Original Investigation 04 December 2001 Pages: 8 - 14
Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate Luca ScapoliMarcella MartinelliPaolo Carinci Original Investigation 10 November 2001 Pages: 15 - 20
The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome René SanterSebastian GrothJürgen Schaub Original Investigation 17 November 2001 Pages: 21 - 29
Rate of homologous chromosome bivalents in spermatocytes may predict completion of spermatogenesis in azoospermic men Leah YogevRonni GamzuHaim Yavetz Original Investigation 16 November 2001 Pages: 30 - 35
Dissecting the epidemiology of a trinucleotide repeat disease – example of FRDA in Finland Vesa JuvonenSatu-Maria KulmalaMarja-Liisa Savontaus Original Investigation 14 November 2001 Pages: 36 - 40
Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs non-Herlitz phenotypes Aoi NakanoSheau-Chiou ChaoJouni Uitto Original Investigation 13 November 2001 Pages: 41 - 51
A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene Tin AungLouise OcakaShomi S. Bhattacharya Original Investigation 23 November 2001 Pages: 52 - 56
Genetic variations in the cholesteryl ester transfer protein gene and high density lipoprotein cholesterol levels in Taiwanese Chinese Lung-An HsuYu-Lin KoYing-Shiung Lee Original Investigation 10 November 2001 Pages: 57 - 63
Cytogenetic mapping of a novel locus for type II Waardenburg syndrome Angelo SelicorniSilvana GuerneriAntonio Pizzuti Original Investigation 10 November 2001 Pages: 64 - 67
Mutations in human glycine N-methyltransferase give insights into its role in methionine metabolism Zigmund LukaRoberto CeroneConrad Wagner Original Investigation 07 December 2001 Pages: 68 - 74
Fetal gender determination in early pregnancy through qualitative and quantitative analysis of fetal DNA in maternal serum Hiroshi HondaNorio MiharuKoso Ohama Original Investigation 23 November 2001 Pages: 75 - 79
Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia Atsushi TajimaI-Hung PanSatoshi Horai Original Investigation 28 November 2001 Pages: 80 - 88
Paraoxonase gene Gln192Arg (Q192R) polymorphism is associated with coronary artery spasm Teruhiko ItoHirofumi YasueHisao Ogawa Original Investigation 06 December 2001 Pages: 89 - 94
The USH1C 216G→A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population Sevtap SavasBen FrischhertzBronya J. Keats Short Report 06 December 2001 Pages: 95 - 97
Critique of “Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension” by Rutherford et al., Human Genetics, published online September 2001 Brian J. Morris Letter to the editors 13 December 2001 Pages: 98 - 99
Authors response to: Critique of "Chromosome 17 and inducible nitric oxide synthase gene in human essential hypertension" by Rutherford et al. in Human Genetics published on-line September 2001 Lyn R. Griffiths Letter to the Editors 13 December 2001 Pages: 100 - 103
Ulrich R. Hengge, Beatrix Volc-Platzer (eds): The skin and gene therapy Rudolf Happle Book Review 10 December 2001 Pages: 104 - 104
Joyce C. Harper, Joy D.A. Delhanty, Alan H. Handyside (eds): Preimplantation genetic diagnosis Francis Flinter Book Review 14 November 2001 Pages: 105 - 106
