Molecular screening and fetal diagnosis of β-thalassemia in the Italian population Maria Cristina RosatelliTeresa TuveriAntonio Cao Review Article Pages: 585 - 589
The majority of the marker chromosomes in Japanese patients with stigmata of turner syndrome are derived from Y chromosomes Shigeo NagafuchiTakashi TamuraYasuo Nakagome Original Investigations Pages: 590 - 592
Identification of a missense phenylketonuria mutation at codon 408 in Chinese Chun-Hung LinKwang-Jen HsiaoTsung-Sheng Su Original Investigations Pages: 593 - 596
No evidence for linkage of familial hypertrophic cardiomyopathy and chromosome 14q1 locus D14S26 in a chinese family: evidence for genetic heterogeneity Yu-Lin KoWen-Pin LienChoong-Chin Liew Original Investigations Pages: 597 - 601
Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation Mark J. PettenatiNagesh RaoIoan T. Thomas Original Investigations Pages: 602 - 606
Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene H. SchefferR. H. J. HouwenC. H. C. M. Buys Original Investigations Pages: 607 - 611
Omission of exon 12 in cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts Ryszard SlomskiManfred SchloesserJochen Reiss Original Investigations Pages: 615 - 619
Physical fine mapping of genes underlying X-linked deafness and non fra(X)-X-linked mental retardation at Xq21 I. BachD. RobinsonF. P. M. Cremers Original Investigations Pages: 620 - 624
A haplotype-linked four base pair deletion upstream of the Aγ globin gene coincides with decreased gene expression Cherif BeldjordRolande DucrocqDominique Labie Original Investigations Pages: 625 - 628
β-Globin gene cluster haplotypes in Yanomama Indians from the Amazon region of Brazil João F. GuerreiroMauro S. FigueiredoMarco A. Zago Original Investigations Pages: 629 - 631
Ornithine transcarbamylase (OTC) deficiency in a female patient with a de novo deletion of the paternal X chromosome Ryszard SlomskiIngrid BraulkeJochen Reiss Original Investigations Pages: 632 - 634
DNA analysis in Turkish Duchenne/Becker muscular dystrophy families Esra BattaloğluMilhan TelatarAshhan Tolun Original Investigations Pages: 635 - 639
A dominant mutation in the COL1A1 gene that substitutes glycine for valine causes recurrent lethal osteogenesis imperfecta Jacky BonaventureLola Cohen-SolalPierre Maroteaux Original Investigations Pages: 640 - 646
Molecular studies of parental origin and mosaicism in 45,X conceptuses Terry HassoldDorothy PettayIrene Uchida Original Investigations Pages: 647 - 652
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene L. OsborneG. SantisR. A. Knight Original Investigations Pages: 653 - 658
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation Heiko TraupeDietmar MüllerHans-Hilger Ropers Original Investigations Pages: 659 - 665
Crossed renal ectopia with pelvic lipomatosis: a new syndrome involving chromosome 1 H. K. GoswamiG. V. RangnekarA. Joshi Original Investigations Pages: 666 - 670
Geographic distribution and genealogy of mutation 207 of the lipoprotein lipase gene in the French Canadian population of Québec Thierry NormandJean BergeronPaul J. Lupien Original Investigations Pages: 671 - 675
Two new human hemoglobin variants caused by unusual mutational events: Hb Zaïre contains a five residue repetition within the α-chain and Hb Duino has two residues substituted in the β-chain H. WajcmanY. BlouquitF. Galacteros Short Communications Pages: 676 - 680
Assignment of the gene for human spasmolytic protein (hSP/SML1) to chromosome 21 Birgit TheisingerCornelius WelterNikolaus Blin Short Communications Pages: 681 - 682
A novel homozygous missense mutation in the protein C (PROC) gene causing recurrent venous thrombosis Catherine B. GrundyMorag ChisholmDavid N. Cooper DNA Variants Pages: 683 - 684
Two different missense mutations at Arg 178 of the protein C (PROC) gene causing recurrent venous thrombosis Catherine B. GrundySam SchulmanDavid N. Cooper DNA Variants Pages: 685 - 686
A HindIII/BglII dystrophin gene polymorphism in the African-American population Thomas W. PriorAudrey C. PappBrian H. Wallace DNA Variants Pages: 687 - 688
A novel NcoI polymorphism creates a fifth haplotype in the 3′ untranslated region of CKM Ann-Marie DifferMartin BobrowChristopher G. Mathew DNA Variants Pages: 689 - 689
No abnormalities in the NAD+ ADP-ribosyltransferase (polymerizing) gene of transformed cells from a Fanconi's anemia patient Karin FlickRainer SchneiderManfred Schweiger Letter to the Editors Pages: 690 - 691