PI LBEI and PI JHOU: two new alpha-1-antitrypsin alleles Qi-long YingChih-chuan LiangMei-lin Zhang Original Investigations Pages: 48 - 50
Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE) B. Kustermann-KuhnK. HarzerJ. Peiffer Original Investigations Pages: 51 - 53
Complementation analysis in lymphoid cells from five patients with different forms of maple syrup urine disease Y. JinnoI. AkaboshiI. Matsuda Original Investigations Pages: 54 - 56
Isolation and subregional mapping of a human cDNA clone detecting a common RELP on chromosome 12 Ivan BalazsMichele PurrelloPaul Szabo Original Investigations Pages: 57 - 61
HLA as a marker of the hemochromatosis gene in Sweden Bernd RitterJan SäfwenbergK. Sigvard Olsson Original Investigations Pages: 62 - 66
The gene for human fibroblast interferon (IFB) maps to 9p21 L. HenryJ. SizunC. Junien Original Investigations Pages: 67 - 69
A unique electrophoretic slow-moving glucose 6-phosphate dehydrogenase variant (G6PD Asahikawa) with a markedly acidic pH optimum T. TakizawaH. FujiiS. Miwa Original Investigations Pages: 70 - 72
The mode of inheritance of psoriasis: Evidence for a major gene as well as a multifactorial component and its implication for genetic counselling Lennart IseliusWick R. Williams Original Investigations Pages: 73 - 76
Pure monosomy and trisomy 2q24.2→q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generations M. MollerD. García-CruzJ. M. Cantú Original Investigations Pages: 77 - 86
The phenotypic effects of small, distal Xq deletions Carolyn TruncaEeva ThermanZ. Rosenwaks Original Investigations Pages: 87 - 89
Two new Bf S subtypes revealed by isoelectric focusing and immunofixation S. WeidingerF. SchwarzfischerH. Cleve Short Communications Pages: 90 - 92
Segregation of two independent chromosomal translocations in one family K. MillerSibylle D. Flatz Clinical Case Reports Pages: 93 - 95
