Identification of carriers of mutant prealbumin gene associated with familial amyloidotic polyneuropathy type I by Southern blot procedures: study of six pedigrees in the Arao district of Japan M. IdeS. MitaS. Araki Original Investigations Pages: 281 - 285
The gene for human apolipoprotein CI is located 4.3 kilobases away from the apolipoprotein E gene on chromosome 19 Ola MyklebostSissel Rogne Original Investigations Pages: 286 - 289
The rate of chromosome breakage is age dependent in lymphocytes of adult controls F. MarlhensW. Al AchkarB. Dutrillaux Original Investigations Pages: 290 - 297
Intensity heteromorphisms of human chromosome 15p by DA/DAPI technique A. BabuM. J. MaceraR. S. Verma Original Investigations Pages: 298 - 300
Clustered GATA repeats (Bkm sequences) on the human Y chromosome J. ArnemannSibylle JakubiczkaJ. T. Epplen Original Investigations Pages: 301 - 303
Bkm sequences are polymorphic in humans and are clustered in pericentric regions of various acrocentric chromosomes including the Y L. SinghK. W. Jones Original Investigations Pages: 304 - 308
Frequency of the fragile X syndrome in Japanese mentally retarded males T. ArinamiI. KondoS. Nakajima Original Investigations Pages: 309 - 312
The isolation of genomic recombinants for the human apolipoprotein B gene and the mapping of three common DNA polymorphisms of the gene —a useful marker for human chromosome 2 N. BarniP. J. TalmudS. E. Humphries Original Investigations Pages: 313 - 319
A routine method for the establishment of permanent growing lymphoblastoid cell lines Heidemarie Neitzel Original Investigations Pages: 320 - 326
Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity E. J. B. M. MensinkA. ThompsonR. K. B. Schuurman Original Investigations Pages: 327 - 332
Studies of a DNA marker (G8) genetically linked to Huntington disease in British families Sandra YoungmanM. SarfaraziJ. F. Gusella Original Investigations Pages: 333 - 339
A polymorphic locus on the long arm of chromosome 20 defined by two probes from a single cosmid M. LittR. SheehyR. E. Magenis Original Investigations Pages: 340 - 345
A subpopulation of t(2;14)(p11;q32) cells in ataxia telangiectasia B lymphocytes S. V. ButterworthA. M. R. Taylor Original Investigations Pages: 346 - 349
Short arm dicentric Y chromosome with associated statural defects in a sterile man Ann C. ChandleyP. AmbrosG. Spowart Original Investigations Pages: 350 - 353
Fine mapping of the Huntington disease linked D4S10 locus by non-radioactive in situ hybridization J. E. LandegentN. Jansen in de WalP. L. Pearson Original Investigations Pages: 354 - 357
First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination E. MornetJ. BouéA. Boué Original Investigations Pages: 358 - 364
The structural gene for the mitochondrial aldehyde dehydrogenase maps to human chromosome 12 T. BraunK. H. GrzeschikH. W. Goedde Short Communications Pages: 365 - 367
A further improved method for identifying heteromorphism of acrocentric chromosomes Tsutomu KameiSei Lee-OkimotoNorio Niikawa Short Communications Pages: 368 - 371
The polymorphism of desialyzed α2HS-glycoptein (AHS): isoelectric focusing in 2.5 M urea as a method for identification of genetic variants K. UmetsuI. YuasaT. Suzuki Short Communications Pages: 372 - 373
Inverted neurons in agyria Cécile BordarierO. RobainCaroline Dhellemes Clinical Case Reports Pages: 374 - 378
“Excess of mental retardation and/or congenital malformation in reciprocal translocations in man” (Fryns et al. 1986) P. Steinbach Letters to the Editors Pages: 379 - 379
