Small metacentric marker chromosomes, particularly isochromosomes, in cancer N. B. AtkinMarion C. Baker Review Pages: 96 - 102
Mutations of the low density lipoprotein receptor in Japanese kindreds with familial hypercholesterolemia Tohru FunahashiYasuko MiyakeBun-ichiro Kishino Original Investigations Pages: 103 - 108
Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease Lindsay A. FarrerBatsheva Bonne-TamirLuigi L. Cavalli-Sforza Original Investigations Pages: 109 - 117
Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients Y. EjimaM. S. SasakiH. Tanooka Original Investigations Pages: 118 - 123
High efficiency in the attribution of parental origin of non-disjunction in trisomy 21 by both cytogenetic and molecular polymorphisms Franca Dagna BricarelliMauro PierluigiNicoletta Sacchi Original Investigations Pages: 124 - 127
Restriction fragment length polymorphisms associated with factor VIII: C gene in Chinese Vivian ChanT. K. ChanA. C. K. Wong Original Investigations Pages: 128 - 131
The ras-related ral gene maps to chromosome 7p15-22 Marie-Françoise Rousseau-MerckAlain BernheimRoland Berger Original Investigations Pages: 132 - 136
Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma Lih-Jiuan S. YoungEva Y. -H. P. LeeWen-Hwa Lee Original Investigations Pages: 137 - 141
Individual specific DNA fingerprints from a hypervariable region probe: alpha-globin 3′HVR Susan J. FowlerPeter GillDouglas R. Higgs Original Investigations Pages: 142 - 146
Acquired chromosome rearrangements in human lymphocytes: effect of aging M. PrieurW. Al AchkarE. Viegas-Péquignot Original Investigations Pages: 147 - 150
Chromosome abnormalities in tuberous sclerosis Susi ScappaticciD. CerimeleM. Fraccaro Original Investigations Pages: 151 - 156
Arabinofuranosyl nucleosides induce common fragile sites Jay C. LeonardRobin C. LeonardKeith H. Thompson Original Investigations Pages: 157 - 162
Agyria — pachygyria and Miller-Dieker syndrome: clinical, genetic and chromosome studies C. DhellemmesS. GirardS. Tapia Original Investigations Pages: 163 - 167
Chromosome localization and polymorphism of an oestrogen-inducible gene specifically expressed in some breast cancers Jean-Paul MoisanMarie-Geneviève MatteiJean-Louis Mandel Original Investigations Pages: 168 - 171
Haemoglobin freiburg: direct detection by synthetic oligonucleotide probes J. HorstR. OehmeE. Kohne Original Investigations Pages: 172 - 174
Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14 Daniel A. RobertsonDavid F. CallenJohn J. Hopwood Original Investigations Pages: 175 - 178
Can sister chromatid intercrossings be considered as prelesions? Carme FusterRosa MiròJosep Egozcue Short Communications Pages: 179 - 180
Human factor H (β1H-globulin): linkage analysis J. KömpfC. LuckenbachH. Ritter Short Communications Pages: 181 - 182
Close linkage of a highly polymorphic marker (D5S37) to familial adenomatous polyposis (FAP) and confirmation of FAP localization on chromosome 5q21-q22 P. Meera KhanC. M. J. TopsF. C. A. den Hartog Jager Short Communications Pages: 183 - 185
Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome Melissa H. LittleDamien B. ThomsonPeter J. Smith Short Communications Pages: 186 - 189
Prenatal diagnosis of alpha-1-antitrypsin deficiency using oligonucleotide probe analysis C. MeisenM. HiguchiK. Olek Short Communications Pages: 190 - 192
Chromosomal rearrangement involving chromosomes 4, 6, 11 and 11 B. EibenW. HammansS. Hansen Case Observed Pages: 193 - 193
Shwachman syndrome and chromosome breakage M. FraccaroSusi ScappaticciM. Aricò Letter to the Editors Pages: 194 - 194