Sperm chromosome analysis in a man heterozygous for a paracentric inversion of chromosome 7 (q11q22) Renee H. Martin Original Investigations Pages: 97 - 100
A product of the C4B locus lacking hemolytic activity Koichi SuzukiGeoffrey J. O'NeillHideo Matsumoto Original Investigations Pages: 101 - 103
Human DNA sequences isolated with an immunoglobulin switch region probe: sequence, chromosomal localization, and restriction fragment length polymorphisms H. StockingerJ. SchmidtkeJ. T. Epplen Original Investigations Pages: 104 - 109
Restriction fragment length polymorphisms associated with immunoglobulin heavy chain gamma genes in Tunisians Hassen ChaabaniN. Torben Bech-HansenDiane W. Cox Original Investigations Pages: 110 - 113
Different baseline sister chromatid exchange levels in density fractionated human lymphocytes Berta Santesson Original Investigations Pages: 114 - 118
Choroideremia-locus maps between DXS3 and DXS11 on Xq A. GalF. BrunsmannI. H. Pawlowitzki Original Investigations Pages: 123 - 126
De novo 21/21 translocation Down syndrome Jovanka NikolišV. Kekić Original Investigations Pages: 127 - 129
The centromere index and relative length of human high-resolution G-banded chromosomes D. L. Van DykeMaria J. WorshamL. Weiss Original Investigations Pages: 130 - 132
Infertility associated with two accessory bisatellited chromosomes M. A. Martín-LucasA. Pérez-CastilloJ. A. Abrisqueta Original Investigations Pages: 133 - 136
Chromosomes in acute nonlymphocytic leukemia E. L. PrigoginaE. W. FleischmanM. A. Frenkel Original Investigations Pages: 137 - 146
Human chromosomal polymorphism A. I. IbraimovM. M. MirrakhimovE. I. Axenrod Original Investigations Pages: 147 - 150
Human chromosomal polymorphism A. I. IbraimovM. M. MirrakhimovG. U. Kurmanova Original Investigations Pages: 151 - 156
Apolipoprotein E3-Leiden. A new variant of human apolipoprotein E associated with familial type III hyperlipoproteinemia L. HavekesElly de WitUlrike Beisiegel Original Investigations Pages: 157 - 163
Studies on three rare fragile sites D. R. RomainL. M. Columbano-GreenC. J. Chapman Original Investigations Pages: 164 - 170
Use of catalase polymorphisms in the study of sporadic aniridia Patricia BoydVeronica van HeyningenN. Hastie Original Investigations Pages: 171 - 174
Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry D. E. WilcoxA. CookeM. A. Ferguson-Smith Original Investigations Pages: 175 - 180
G-banding of human sperm chromosomes J. BenetA. GenescàC. templado Short Communications Pages: 181 - 182
Genetic polymorphism of coagulation factor XIII B subunit in the Japanese population: description of three new rare alleles Shigeki NakamuraOsamu OhueKazue Abe Short Communications Pages: 183 - 185
DNA-diagnosis of sickle cell anemia from chorionic villi: possible influence of maternal cell contamination Renate OehmeW. -D. JonathaJ. Horst Short Communications Pages: 186 - 187
Maternal 3:1 disjunction in a tranlocation 9/17 M. A. Sánchez FerrerM. L. de TorresJ. A. Abrisqueta Cases Observed Pages: 188 - 188