A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones Susanne PoppAnna JauchThomas Cremer Original Investigations Pages: 527 - 532
Topographic pattern of the rearrangement of the dystrophin gene in Japanese Duchenne muscular dystrophy Natsuki ImotoTadao ArinamiHitoshi Takita Original Investigations Pages: 533 - 536
High degree of genetic polymorphism in apolipoprotein(a) associated with plasma lipoprotein(a) levels in Japanese and Chinese populations Shuichi KikuchiAkiko NakagawaHideo Hamaguchi Original Investigations Pages: 537 - 544
Frequent occurrence of familial aggregations of high lipoprotein(a) levels associated with small apolipoprotein(a) isoforms Hisako YanagiAkiko NakagawaHideo Hamaguchi Original Investigations Pages: 545 - 548
Acute intermittent porphyria caused by a G to C mutation in exon 12 of the porphobilinogen deaminase gene that results in exon skipping Makoto DaimonKeiichi YamataniHideo Sasaki Original Investigations Pages: 549 - 553
Analysis of 6 VNTR loci by ‘multiplex’ PCR and automated fluorescent detection Gillian TullyKevin M. SullivanPeter Gill Original Investigations Pages: 554 - 562
Localization of the gene for human heart fatty acid binding protein to chromosome 1p32-1p33 Robert F. TroxlerGwynneth D. OffnerHerman E. Wyandt Original Investigations Pages: 563 - 566
South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch population J. C. DefescheD. E. van DiermenJ. J. P. Kastelein Original Investigations Pages: 567 - 570
Familial true hermaphroditism: paternal and maternal transmission of true hermaphroditism (46,XX) and XX maleness in the absence of Y-chromosomal sequences U. KuhnleH. P. SchwarzA. Braun Original Investigations Pages: 571 - 576
Somatic pairing of centromeres and short arms of chromosome 15 in the hematopoietic and lymphoid system Jerry P. LewisHans J. TankeHanneke C. Kluin-Nelemans Original Investigations Pages: 577 - 582
Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19 Marie-Françoise Rousseau-MerckJosette HillionRoland Berger Original Investigations Pages: 583 - 587
RFLP haplotyping and mutation analysis of the phenylalanine hydroxylase gene in Dutch phenylketonuria families Henk MeijerRoselie J. E. JongbloedJoep P. M. Geraedts Original Investigations Pages: 588 - 592
Allele frequencies and linkage disequilibrium of polymorphic DNA markers of the Huntington disease region in the German population Ulrike ThiesBarbara BockelKirsten Schröder Original Investigations Pages: 593 - 597
Logistic regression model to estimate the risk of unbalanced offspring in reciprocal translocations Christine CansOlivier CohenPierre Jalbert Original Investigations Pages: 598 - 604
Von Hippel-Lindau disease: identification of deletion mutations by pulsed-field gel electrophoresis Masahiro YaoFarida LatifBerton Zbar Original Investigations Pages: 605 - 614
The human cytochrome b5 gene and two of its pseudogenes are located on chromosomes 18q23, 14q31-32.1 and 20p11.2, respectively Sara J. GiordanoMin YooAlan W. Steggles Original Investigations Pages: 615 - 618
Detection of a high mutation frequency in exon 12 of the porphobilinogen deaminase gene in patients with acute intermittent porphyria C. S. MgoneW. G. LanyonJ. M. Connor Original Investigations Pages: 619 - 622
Generation of a chromosome-22-specific c-DNA library as confirmed by FISH analysis Elisabeth GöttertVeronika KleinEckart Meese Original Investigations Pages: 623 - 626
Rapid detection of single nucleotide deletions: application to the β 6 (-A) mutation of the β-globin gene and to cystic fibrosis Marie-Catherine RomeyPatricia Aguilar-MartinezMireille Claustres Short Communications Pages: 627 - 628
Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25 Olaf RiessCornelia EpplenJörg T. Epplen Short Communications Pages: 629 - 630
An EcoRI RFLP in the 5′ region of the human NF1 gene E. ReyniersK. De BoulleP. J. Willems OriginalPaper Pages: 631 - 631
EcoRI restriction fragment length polymorphism in human glycogen synthase gene Suzanne A. AdjoaClaude BouchardFrance T. Dionne OriginalPaper Pages: 632 - 632
A common exonic polymorphism in the human D5 dopamine receptor gene Steve S. SommerJanet L. SobellLeonard L. Heston OriginalPaper Pages: 633 - 634
Sequence variability of the tetranucleotide repeat of the human beta-actin related pseudogene H-beta-Ac-psi-2 (ACTBP2) locus Andy UrquhartColin P. KimptonPeter Gill OriginalPaper Pages: 637 - 638
Human fibronectin gene (FN1) RFLPs: Mapping and linkage disequilibrium analysis Rita GardellaMarina ColombiSergio Barlati OriginalPaper Pages: 639 - 641
Oocyte selection model for the maternal age-dependence in Down syndrome Andrew D. Carothers Letters to the Editors Pages: 642 - 643
