Werner's syndrome: A review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations Darrell Salk Review Article Pages: 1 - 15
Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's syndrome Susi ScappaticciD. CerimeleM. Fraccaro Original Investigations Pages: 16 - 24
High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequency D. CerimeleF. CottoniM. Fraccaro Original Investigations Pages: 25 - 30
The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromes Robert S. YoungTerry ReedCatherine G. Palmer Original Investigations Pages: 31 - 39
Pathogenetic significance of “pure” monosomy 7 in myeloproliferative disorders. analysis of 14 cases F. PasqualiP. BernasconiR. Sanger Original Investigations Pages: 40 - 51
X-Linked Leigh's syndrome Paul J. BenkeJoseph C. Parker Jr.Anne E. Feuer Original Investigations Pages: 52 - 59
Relationship between behavioral maturation measured by the “Baum” test and EEG frequency. A pilot study on monozygotic and dizygotic twins F. VogelEdda SchaltG. Klarich Original Investigations Pages: 60 - 65
Evidence for the deficiency of β-glucosidase-activating factor in fibroblasts of patients with I-cell disease Raymonda VaronWillem J. KleijerAlessandra d'Azzo Original Investigations Pages: 66 - 69
Sperm aging in the male and cytogenetic anomalies. An animal model Patricia A. Martin-DeLeonMelinda L. Boice Original Investigations Pages: 70 - 77
Abnormal blood group galactosyltransferase in blood type A1B-subjects whose sera contain anti-B agglutinin Akira YoshidaVibha Davé Original Investigations Pages: 78 - 81
Familial lecithin-cholesterol acyltransferase deficiency in a Japanese family: Evidence for functionally defective enzyme in homozygotes and obligate heterozygotes John J. AlbersChing-Hong ChenYasuo Akanuma Original Investigations Pages: 82 - 85
Polymorphism of BF, C2, and GLO in Japanese patients with insulin-dependent diabetes mellitus: Confirmation of an increase of BF *FT Katsushi TokunagaKeiichi OmotoTokuji Itoh Original Investigations Pages: 86 - 88
The isochromosome (17q) in chronic myelocytic leukaemia: Mechanism of origin, centromeric function and clonal evolution F. PasqualiC. PanarelloR. Casalone Short Communications Pages: 89 - 90
Glyoxalase I polymorphism and racial admixture in the Cuban population M. GarcíaM. EstradaR. González Short Communications Pages: 91 - 92
The turner phenotype and the different types of human X isochromosome Daniela LarizzaGiuseppina AbbatiFrancesca Severi Letter to the Editor Pages: 93 - 93
