Microsatellite variation and the differentiation of modern humans Anna Pérez-LezaunFrancesc CalafellJ. Bertranpetit Original investigation Pages: 1 - 7
An asymptomatic germline missense base substitution in the hypoxanthine phosphoribosyltransferase (HPRT) gene that reduces the amount of enzyme in humans S. FujimoriRyozo SakumaNaoyuki Kamatani Original investigation Pages: 8 - 10
Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes B. HuangJ. A. CrollaD. H. Ledbetter Original investigation Pages: 11 - 17
Molecular evidence for human alpha2-HS glycoprotein (AHSG) polymorphism M. OsawaKazuo UmetsuSanae Takeichi Original investigation Pages: 18 - 21
Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families D. F. WyszynskiNancy MaestriTerri H. Beaty Original investigation Pages: 22 - 26
Microsatellite polymorphism of the α1-antichymotrypsin gene locus associated with sporadic Alzheimer’s disease Kevin MorganLinda MorganN. A. Kalsheker Original investigation Pages: 27 - 31
Localization of the human HuR gene to chromosome 19p13.2 Wei-Jun MaH. Furneaux Original investigation Pages: 32 - 33
Amplified product length polymorphism (APLP): a novel strategy for genotyping the ABO blood group Gotaro WatanabeKazuo UmetsuT. Suzuki Original investigation Pages: 34 - 37
Allelic variants of human calcitonin receptor in the Japanese population M. NakamuraZhi-qiang ZhangKennichi Kakudo Original investigation Pages: 38 - 41
Analysis of chromosomal equipment in spermatozoa of a 46,XY/47,XY/+8 male by means of multicolour fluorescent in situ hybridization: confirmation of a mosaicism and evaluation of risk for offspring S. MercierJean Luc Bresson Original investigation Pages: 42 - 46
Latent chromosomal instability in cancer patients Maria TzanchevaD. Komitowski Original investigation Pages: 47 - 51
Possible control of dopamine β-hydroxylase via a codominant mechanism associated with the polymorphic (GT)n repeat at its gene locus in healthy individuals J. WeiC. N. RamchandGwynneth P. Hemmings Original investigation Pages: 52 - 55
Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms K. Brøndum-NielsenBente BeckNiels Tommerup Original investigation Pages: 56 - 61
PCR-based detection of mosaicism in Turner syndrome patients T. YorifujiJunko MuroiKenshi Furusho Original investigation Pages: 62 - 65
Genetic polymorphisms of the renin-angiotensin system and angiographic extent and severity of coronary artery disease: the CORGENE study X. JeunemaitreFrançois LedruPierre Ducimetière Original investigation Pages: 66 - 73
Prevalence of ΔF508 cystic fibrosis carriers in The Netherlands: logistic regression on sex, age, region of residence and number of offspring H. G. de VriesJ. Margriet ColléeL. P. ten Kate Original investigation Pages: 74 - 79
Refined localization of the pyruvate dehydrogenase E1α gene (PDHA1) by linkage analysis A. D. BørglumTracey FlintT. A. Kruse Original investigation Pages: 80 - 82
X-linked adrenal hypoplasia in a large Greenlandic family. Detection of a missense mutation (N440I) in the DAX-1 gene; implication for genetic counselling and carrier diagnosis M. SchwartzSusanne BlichfeldtJørn Müller Original investigation Pages: 83 - 87
Mutational and functional analysis of the neurofibromatosis type 1 (NF1) gene M. UpadhyayaMichael J. OsbornDavid N. Cooper Original investigation Pages: 88 - 92
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A gene A. SavoiaMaria Rosaria PiemonteseLeopoldo Zelante Original investigation Pages: 93 - 97
Mutations in the gene encoding 21-hydroxylase detected by solid-phase minisequencing G. OhlssonMarianne Schwartz Original investigation Pages: 98 - 102
The high mobility group I-C gene (HMGI-C): polymorphism and genetic localization C. S. IshwadM. D. ShriverR. E. Ferrell Original investigation Pages: 103 - 105
The T705I mutation of the low density lipoprotein receptor gene (FH Paris-9) does not cause familial hypercholesterolemia P. LombardiEric J. G. SijbrandsLouis M. Havekes Original investigation Pages: 106 - 107
Association between common alleles of the low-density lipoprotein receptor gene region and interindividual variation in plasma lipid and apolipoprotein levels in a population-based sample from Rochester, Minnesota M. B. HavilandR. E. FerrellC. F. Sing Original investigation Pages: 108 - 114
Refinement of the dominant optic atrophy locus (OPA1) to a 1.4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contig A. JonasdottirHans EibergThomas Rosenberg Original investigation Pages: 115 - 120
Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutations Maria TzetisE. KanavakisChristos Kattamis Original investigation Pages: 121 - 125
Molecular basis of variegate porphyria: a de novo insertion mutation in the protoporphyrinogen oxidase gene H.-M. LamLaryssa DraganA. M. Christiano Original investigation Pages: 126 - 129
Exclusion of the phosphoinositide-specific phospholipase Cβ3 (PLCB3) gene as a candidate for multiple endocrine neoplasia type 1 Günther WeberSean GrimmondCatharina Larsson Original investigation Pages: 130 - 132
Exclusion of the phosphatidylinositol-specific phospholipase C β3 (PLC β3) gene as candidate for the multiple endocrine neoplasia type 1 (MEN 1) gene Mireille J. de WitRudy M. LandsvaterMireille J. de Wit Original investigation Pages: 133 - 137
The IGHG3 gene shows a structural polymorphism characterized by different hinge lengths: sequence of a new 2-exon hinge gene Patricia DardSylvie HuckA. Sanchez-Mazas Rapid communication Pages: 138 - 141