Diagnosis of genetic disease using recombinant DNA D. N. CooperJ. Schmidtke Review Articles Pages: 1 - 11
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function Diletta PerettiPaola MaraschioOrsetta Zuffardi Original Investigations Pages: 12 - 16
Assignment of the human γ-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33–36 Y. ShilohT. DonlonLap-Chee Tsui Original Investigations Pages: 17 - 19
The effect of caffeine on fragile X expression M. A. AbruzzoDorothy PettayPatricia A. Jacobs Original Investigations Pages: 20 - 22
Characteristics and distribution of β thalassemia haplotypes in South China Vivian ChanT. K. ChanD. Todd Original Investigations Pages: 23 - 26
The frequency of false-positive and false-negative results in the detection of Y-chromosomes in interphase nuclei J. L. ThomsenE. Niebuhr Original Investigations Pages: 27 - 30
β-Globin gene polymorphism in the Saudi Arab population M. A. F. El-Hazmi Original Investigations Pages: 31 - 34
Ganglioside GM1 metabolism in living human fibroblasts with β-galactosidase deficiency G. M. S. ManciniA. T. HoogeveenL. Svennerholm Original Investigations Pages: 35 - 38
Familial lethal sleep apnea F. D. AdickesB. A. BuehlerW. G. Sanger Original Investigations Pages: 39 - 43
Premature chromosome condensation —studies on human metastatic carcinoma cells Silke BrüderleinE. GebhartMeena Augustus Original Investigations Pages: 44 - 52
Heterozygosity for phosphodiester glycosidase deficiency: a novel human mutation of lysosomal enzyme processing D. AlexanderMarlene DeebF. Talj Original Investigations Pages: 53 - 59
Maternal serum alpha-fetoprotein screening for neural tube defects and other disorders using an ultramicro-ELISA Hannelore KörnerLidia RodriguezH. Günther Original Investigations Pages: 60 - 63
The proα2 (V) collagen gene (COL5A2) maps to 2q14→2q32, syntenic to the proα1 (III) collagen locus (COL3A1) Cécile Huerre-JeanpierreIsabelle HenryClaudine Junien Original Investigations Pages: 64 - 67
A multipoint linkage analysis program for X-linked disorders, with the example of Duchenne muscular dystrophy and seven DNA probes J. Clayton Original Investigations Pages: 68 - 72
In situ hybridization studies on variant t(2;8) translocations in Burkitt lymphoma lines H. HameisterSabine Adolph Original Investigations Pages: 73 - 76
The genes for human gastrin and cholecystokinin are located on different chromosomes T. LundA. H. M. Geurts van KesselJ. E. Dixon Original Investigations Pages: 77 - 80
Adaptation-like response to the chemical induction of sister chromatid exchanges in human lymphocytes K. MorimotoM. Sato-MizunoA. Koizumi Original Investigations Pages: 81 - 85
Clastogen-induced chromosomal breakage as a marker for first trimester prenatal diagnosis of Fanconi anemia Arleen D. AuerbachZhang MinJoëlle Boué Short Communications Pages: 86 - 88
Extended polymorphism of the human esterase D isozyme system: description of a “new” allele EsD*11 J. HenkeH. SchweitzerM. P. Baur Short Communications Pages: 89 - 90
Length polymorphism in the pro α2(I) collagen gene: an alternative explanation in a case of Marfan syndrome R. DalgleishG. WilliamsJ. R. Hawkins Short Communications Pages: 91 - 92
Apert syndrome and fetal hydrocephaly Hyon KimVijay UppalR. Wallach Clinical Case Reports Pages: 93 - 95
