Interstitial deletion of chromosome 6q: Precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting N. RubtsovG. SengerH. Kuzcera Original Investigation Pages: 705 - 709
Extreme variant of the short arm of chromosome 15 U. FriedrichA. J. TherkelsenE. Niebuhr Original Investigation Pages: 710 - 713
Allelic association between a Ser-9-Gly polymorphism in the dopamine D3 receptor gene and schizophrenia S. ShaikhD. A. CollierM. Gill Original Investigation Pages: 714 - 719
Localization of the humanRGR opsin gene to chromosome 10q23 X. -N. ChenJ. R. KorenbergH. K. W. Fong Original Investigation Pages: 720 - 722
Novel interleukin-1 receptor antagonist exon polymorphisms and their use in allele-specific mRNA assessment F. E. ClayJ. K. TarlowG. W. Duff Original Investigation Pages: 723 - 726
Geographic distribution and origin of CFTR mutations in Germany B. TümmlerT. StorrsX. Estivill Original Investigation Pages: 727 - 731
Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11g13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene J. T. PangS. E. LloydR. T. Taggart Original Investigation Pages: 732 - 741
EagI andNotI linking clones from human chromosomes 11 and Xp Mark A. PookRekhaben ThakrarRajesh V. Thakker Original Investigation Pages: 742 - 749
Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cells V. P. SchulzV. A. ZakianS. D. Edland Original Investigation Pages: 750 - 754
Hereditary ceruloplasmin deficiency with hemosiderosis N. OkamotoS. WadaY. Wada Original Investigation Pages: 755 - 758
Distribution and frequency of a polymorphicAlu insertion at the plasminogen activator locus in humans S. A. TishkoffG. RuanoK. K. Kidd Original Investigation Pages: 759 - 764
Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalities Yi NingMarjorie RosenbergLeslie G. Biesecker Original Investigation Pages: 765 - 769
Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation Hans-Jochen H. DeckerChristine NeuhausChristoph Huber Original Investigation Pages: 770 - 776
Extensive polymorphism of ABO blood group gene: three major lineages of the alleles for the common ABO phenotypes Kenichi OgasawaraMakoto BannaiKatsushi Tokunaga Original Investigation Pages: 777 - 783
Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10) M. ErdelS. KöchlU. Barth-Witte Original Investigation Pages: 784 - 793
Localization of the human vascular endothelial growth factor gene,VEGF, at Chromosome 6p12 M. -H. WeiN. C. PopescuM. J. Merrill Original Investigation Pages: 794 - 797
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13 A. CamuzatJ. -M. RozetJ. Weissenbach Original Investigation Pages: 798 - 801
Familial double pericentric inversion of chromosome 5 with some features of cri-du-chat syndrome Sheryl A. GoodartMerlin G. ButlerJoan Overhauser Original Investigation Pages: 802 - 807
A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males Luciana A. HaddadRegina C. Mingroni-NettoSérgio D. J. Pena Original Investigation Pages: 808 - 812
Allele-specific quantification of TNFA transcripts in rheumatoid arthritis Brigitta M. N. BrinkmanTom W. J. HuizingaCornelis L. Verweij Original Investigation Pages: 813 - 818
The effect of Y-chromosome alpha-satellite array length on the rate of sex chromosome disomy in human sperm Michael A. AbruzzoDarren K. GriffinTerry J. Hassold Original Investigation Pages: 819 - 823
A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus Patricia SmeyersEugènia MonrósFrancesc Palau Original Investigation Pages: 824 - 828
Hb Costa Rica or α2β277(EF1)His→Arg: The first example of a somatic cell mutation in a globin gene W. E. Rodriguez RomeroM. CastilloT. H. J. Huisman Original Investigation Pages: 829 - 833
Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus Huib CaronPeter van SluisRogier Versteeg Original Investigation Pages: 834 - 837
A novel 5′-upstream mutation in the factor X11 gene is associated with a Taql restriction site in an Alu repeat in factor X11-deficient patients Sigrun HofferbertJens MüllerManfred Schloesser Rapid Communication Pages: 838 - 841
Six new polymorphic microsatellite markers used for the integration of genetic and physical maps of human chromosome 7 Simone BeckFarah BadbanchiKarl-Heinz Grzeschik Rapid Communication Pages: 842 - 844
Hb Costa Rica or · 2 ‚ 277(EF1)His→Arg: the first example of a somatic cell mutation in a globin gene W. E. Rodriguez RomeroM. CastilloT. H. J. Huisman Original investigation Pages: 829 - 833