Chromosome aberrations in psoriatic patients treated with arsenic I. NordensonS. SalmonssonG. Beckman Original Investigations Pages: 1 - 6
Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents Ségolène AymeMarie-Geneviève MatteiF. Giraud Original Investigations Pages: 7 - 12
Regional assignment of red cell acid phosphatase locus to band 2p25 Claudine JunienJ.-C. KaplanR. Berger Original Investigations Pages: 17 - 21
Relationship between α-L-fucosidase deficiency in plasma and α-L-fucosidase activity in leukocytes Rosanna GattiSilvia CavalieriGiovanni Romeo Original Investigations Pages: 23 - 30
Characteristics of galactokinase and galactose-1-phosphate uridyltransferase in cultivated fibroblasts and amniotic fluid cells Yoon Shin-BuehringH. LeitnerJ. Schaub Original Investigations Pages: 31 - 37
Nucleolus organiser regions on mitotic and meiotic chromosomes from infertile males investigated using a specific silver stain J. IronsideM. J. W. Faed Original Investigations Pages: 39 - 43
Familial XX true hermaphroditism and the H-Y antigen M. FraccaroL. TiepoloU. Wolf Original Investigations Pages: 45 - 52
The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(qh′,RHG,GAG,CBG) E. DontiG. VentiF. Pimpinelli Original Investigations Pages: 53 - 59
18q- Syndrome resulting from a tdic(14p;18q) J. C. LambertMartine FerrariN. Ayraud Original Investigations Pages: 61 - 66
Down's syndrome in Western Australia: Cytogenetics and incidence Marie T. Mulcahy Original Investigations Pages: 67 - 72
Sister chromatid exchange and cell cycle in fibroblasts of Bloom's syndrome S. Ved Brat Original Investigations Pages: 73 - 79
Serum protein polymorphisms in a village community from the Gambia, West Africa (Hp, Tf, and Gc) S. G. WelchC. A. SwindlehurstK. Williams Original Investigations Pages: 81 - 84
Single Cd band in dicentric translocations with one suppressed centromere A. Daniel Original Investigations Pages: 85 - 92
Phosphofructokinase (PFK) isozymes in man Axel KahnMarie-Claire MeienhoferJean-Claude Dreyfus Original Investigations Pages: 93 - 108
Chronic myelogenous leukemia with an unusual karyotype Anna PananiA. G. PapayannisC. Gardikas Short Communications Pages: 109 - 111
Periodic hypokalemic paralysis transmitted by an unaffected male with negative family history: A delayed mutation? H. H. RopersH. B. Szliwowski Short Communications Pages: 113 - 116
X-Linked mental retardation with macro-orchidism and the fragile site at Xq27 or 28 G. R. SutherlandP. L. C. Ashforth Short Communications Pages: 117 - 120
Los Angeles variant of galactose-1-phosphate uridyltransferase (EC 2.7.7.12) in a Mexican family B. IbarraG. VacaJ. M. Cantú Short Communications Pages: 121 - 124
Improved technique for human leukocyte cultures Julie R. Korenberg Short Communications Pages: 125 - 126
Interstitial delection of the long arm of chromosome 8 J. P. FrynsN. LoggheH. Van Den Berghe Clinical Case Reports Pages: 127 - 130
Fragile site long arm chromosome 16 K. SørensenJ. NielsenJ. Haahr Clinical Case Reports Pages: 131 - 134
Partial long arm deletion of one X chromosome in a patient with secondary amenorrhea U. RuthnerS. MaschikG. Breitenecker Clinical Case Reports Pages: 135 - 137
A case of long arm deletion of the X chromosome in a patient with secondary amenorrhea S. BrankovićŽ. LaćaS. Morić-Petrović Clinical Case Reports Pages: 139 - 142