An alphoid DNA sequence conserved in all human and great ape chromosomes: evidence for ancient centromeric sequences at human chromosomal regions 2q21 and 9q13 Antonio BaldiniThomas RiedDavid C. Ward Original Investigations Pages: 577 - 583
Detection of amplified DNA sequences by reverse chromosome painting using genomic tumor DNA as probe Stefan JoosHarry ScherthanPeter Lichter Original Investigations Pages: 584 - 589
Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization Stanislas du ManoirMichael R. SpeicherThomas Cremer Original Investigations Pages: 590 - 610
Hypomelanosis of Ito in a girl with plexus papilloma and translocation (X;17) E. Steichen-GersdorfR. TrawögerG. Utermann Original Investigations Pages: 611 - 613
A null allele frequent in non-Jewish Tay-Sachs patients Saïd AkliJamel ChellyLivia Poenaru Original Investigations Pages: 614 - 620
A single amino acid deletion in the α2(I) chain of type I collagen produces osteogenesis imperfecta type III Karen MolyneuxBarbra J. StarmanRaymond Dalgleish Original Investigations Pages: 621 - 628
Prothymosin α gene in humans: organization of its promoter region and localization to chromosome 2 P. SzaboC. PanneerselvamB. L. Horecker Original Investigations Pages: 629 - 634
Human breast cancer: frequent p53 allele loss and protein overexpression S. SinghM. SimonH. W. Goedde Original Investigations Pages: 635 - 640
An α-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the αV/41 polymorphism N. Dalla VeneziaR. WilmotteJ. Delaunay Original Investigations Pages: 641 - 644
A missense mutation, S349P, completely inactivates phenylalanine hydroxylase in North African Jews with phenylketonuria Michal WeinsteinRandy C. EisensmithYosef Shiloh Original Investigations Pages: 645 - 649
Identification of an alternative 5′ untranslated region of the adenomatous polyposis coli gene Sylvia LambertzWolfgang G. Ballhausen Short Communications Pages: 650 - 652
Regional assignment of the gene coding for a human Graves' disease autoantigen to 10q21.3–q22.1 Elena RossiRaffaele ZarrilliOrsetta Zuffardi Short Communications Pages: 653 - 654
Genetic and population study of a Y-linked tetranucleotide repeat DNA polymorphism with a simple non-isotopic technique Fabrício R. SantosSergio D. J. PenaJörg T. Epplen Short Communications Pages: 655 - 656
Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome Anne MonclaLuciana PirasMichel Fontes Short Communications Pages: 657 - 660
A study of the genetic polymorphism of human inter-alpha-trypsin-inhibitor (ITI) in the Han population, Chengdu, China Hou YipingGou QingWu Meiyun Short Communications Pages: 661 - 662
Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization C. DesmazeP. ScamblerA. Aurias Short Communications Pages: 663 - 665
An RFLP for probe 26-6 that is useful in linkage diagnosis for adult polycystic kidney disease Stephen JefferyStephen Morgan OriginalPaper Pages: 666 - 667
A sequence variation in the human cystatin D gene resulting in an amino acid (Cys/Arg) polymorphism at the protein level Milagros BalbínJosé P. FreijeCarlos López-Otín OriginalPaper Pages: 668 - 669
