Flow cytometric and cytogenetic analyses in human spontaneous abortions Raffaele De VitaAlberto CalugiAntonio Vizzone Original Investigations Pages: 409 - 415
Reevaluation of the chromosome 4q candidate region for early onset periodontitis Thomas C. HartMary L. MarazitaScott R. Diehl Original Investigations Pages: 416 - 422
Analysis of a genetic mutation in an electrophoretic variant of the human lactate dehydrogenase-B(H) subunit Masato MaekawaKayoko SudoTakashi Kanno Original Investigations Pages: 423 - 426
Fetal nucleated cells in maternal peripheral blood: frequency and relationship to gestational age Hiromi HamadaTadao ArinamiHirokazu Iwasaki Original Investigations Pages: 427 - 432
Structure and expression analysis of a member of the human glutamate dehydrogenase (GLUD) gene family mapped to chromosome 10p11.2 George TzimagiorgisMargaret A. LevershaNicholas K. Moschonas Original Investigations Pages: 433 - 438
SSCP detection of a Gly565Val substitution in the proα(I) collagen chain resulting in osteogenesis imperfecta type II Katrina MackayAllan M. LundRaymond Dalgleish Original Investigations Pages: 439 - 444
Demographic reductions and genetic bottlenecks in humans: minisatellite allele distributions in oceania J. J. MartinsonR. M. HardingJ. B. Clegg Original Investigations Pages: 445 - 450
Identification of two new nucleotide mutations (HPRTUtrecht and HPRTMadrid) in exon 3 of the human hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene Anne G. M. Bouwens-RomboutsMarie-Jose H. van den BoogaardMarcel G. J. Tilanus Original Investigations Pages: 451 - 454
Loss of heterozygosity on chromosome 11p13 in primary bladder carcinoma R. ShipmanP. SchramlC. U. Ludwig Original Investigations Pages: 455 - 458
Increased chromosome fragility in lymphocytes of short normal children treated with recombinant human growth hormone Bruna TedeschiGian Luigi SpadoniBrunetto Boscherini Original Investigations Pages: 459 - 463
Inter-ethnic polymorphism of the β-globin gene locus control region (LCR) in sickle-cell anemia patients Bruno PérichonAngela RagusaRajagopal Krishnamoorthy Original Investigations Pages: 464 - 468
Between-generation differences in ascertainment and penetrance: relevance to genetic hypotheses in fragile X Danuta Z. LoeschLeslie J. SheffieldDavid A. Hay Original Investigations Pages: 469 - 474
The human apolipoprotein B 3′ hypervariable region: detection of eight new alleles and comparisons of allele frequencies in blacks and whites James E. HixsonPatricia K. PowersC. Alex McMahan Original Investigations Pages: 475 - 479
Identification of a splice-site mutation in the low density lipoprotein receptor gene by denaturing gradient gel electrophoresis Bert TopAndré van der ZeeRune R. Frants Original Investigations Pages: 480 - 484
Physical mapping in the region of human Xq12-21.1 using pulsed field gel electrophoresis Alison M. JonesSue MalcolmChristine Kinnon Original Investigations Pages: 485 - 488
Analysis of human extrachromosomal DNA elements originating from different β-satellite subfamilies Günter AssumThomas FinkKarl J. Fisel Original Investigations Pages: 489 - 495
The pattern of spontaneous germ-line mutation: relative rates of mutation at or near CpG dinucleotides in the factor IX gene Cynthia D. K. BottemaRhett P. KetterlingSteve S. Sommer Original Investigations Pages: 496 - 503
Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13 R. Frank KooyAnneke Y. Van der VeenCharles H. C. M. Buys Short Communications Pages: 504 - 506
Molecular abnormality of G6PD Konan and G6PD Ube, the most common glucose-6-phosphate dehydrogenase variants in Japan Akira HironoHisaichi FujiiShiro Miwa Short Communications Pages: 507 - 508
A new polymorphic restriction site at the human atrial natriuretic peptide (hANP) gene locus Rajendranath RamasawmyNavaratnam KoteaRajagopal Krishnamoorthy OriginalPaper Pages: 509 - 510
Two new polymorphisms in the coding sequence of the LDL receptor (LDLR) gene B. Saint-JoreN. LouxC. Boileau OriginalPaper Pages: 511 - 512
A frequent EcoRI polymorphism in the bcl-2 gene Paolo GhiaIrma DianzaniFederico Caligaris-Cappio OriginalPaper Pages: 513 - 513
Choroid plexus cysts diagnosed prenatally as an independent risk factor for cytogenetic abnormality Ernest B. Hook Letters to the Editors Pages: 514 - 514
H-Y (SDM) antibody specifically binds Müllerian inhibiting substance Ulrich MüllerStephen S. WachtelEllen H. Goldberg Letters to the Editors Pages: 514 - 515
Hereditary hydronephrosis and the short arm of chromosome 6 J. P. FrynsA. KleczkowskaK. Vandenberghe Letters to the Editors Pages: 515 - 518