Localization of the LDHA gene to 11p14→11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13 T. L. Yang-FengG. A. P. BrunsU. Francke Original Investigations Pages: 331 - 334
In vivo chromosomal instability in ataxia-telangiectasia homozygotes and heterozygotes Miriam P. RosinH. D. Ochs Original Investigations Pages: 335 - 340
The plasminogen polymorphism in South African Negro populations: genetics and anthropogenetics H. W. HitzerothUlrike SkodaG. Mauff Original Investigations Pages: 341 - 345
Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84 T. CremerJ. LandegentM. van der Ploeg Original Investigations Pages: 346 - 352
Measurements of the frequency of human erythrocytes with gene expression loss phenotypes at the glycophorin A locus R. G. LangloisW. L. BigbeeR. H. Jensen Original Investigations Pages: 353 - 362
Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis D. DhermyM. GarbarzP. Boivin Original Investigations Pages: 363 - 367
An elongated segment of DNA observed between two human α globin genes T. NakatsujiH. LandmanT. H. J. Huisman Original Investigations Pages: 368 - 371
Molecular detection of a translocation (Y;15) in a 45,X male C. M. DistecheL. BrownD. C. Page Original Investigations Pages: 372 - 377
Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells F. ArwertH. J. PorckA. W. Eriksson Original Investigations Pages: 378 - 381
Congenital malformations and genetic diseases in Iranian infants D. D. FarhudGh. -R. WalizadehM. Sharif Kamali Original Investigations Pages: 382 - 385
Severe short-limb dwarfism resembling Grebe chondrodysplasia Ahmad S. TeebiSadika A. Al-AwadiJ. Spranger Original Investigations Pages: 386 - 390
Localisation of the gene for Hunter syndrome on the long arm of X chromosome M. UpadhyayaM. SarfaraziP. S. Harper Original Investigations Pages: 391 - 398
Chromosome studies in 2136 couples with spontaneous abortions G. BourrouillouP. ColombiesN. Dastugue Original Investigations Pages: 399 - 401
Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency E. MornetP. CouillinJ. Dausset Original Investigations Pages: 402 - 408
A linkage study of Emery-Dreifuss muscular dystrophy Shirley HodgsonErnst BoswinkelM. Bobrow Original Investigations Pages: 409 - 416
Partial trisomy 20p resulting from a recombination of a familial pericentric inversion N. BownI. CrossJ. Burn Original Investigations Pages: 417 - 419
Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14–q21 M. G. MatteiY. ColinJ. P. Cartron Original Investigations Pages: 420 - 422
New regional localisations for HAGH and PGP on human chromosome 16 J. C. MulleyD. F. Callen Original Investigations Pages: 423 - 424
A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library L. BuftonT. K. MohandasM. Litt Original Investigations Pages: 425 - 431
Alpha-thalassemia in Papua New Guinea P. YenchitsomanusK. M. SummersG. T. Nurse Original Investigations Pages: 432 - 437
Oxygen-induced cytogenetic instability in normal human lymphocytes H. JoenjeAnneke B. Oostra Original Investigations Pages: 438 - 440
Prematurely condensed human sperm chromosomes after in vitro fertilization (IVF) H. SchmiadyK. SperlingM. Stauber Original Investigations Pages: 441 - 443
The effect of 1-β-d-arabinofuranosyl-cytosine on the expression of the common fragile site at 3p14 Xinzhi LiZu-an YanXianting Zhou Original Investigations Pages: 444 - 446
Aberrant breakpoints in chronic myelogenous leukaemia; oncogenes and fragile sites J. L. HuretJ. TanzerM. Henry-Amar Original Investigations Pages: 447 - 448
Choroideremia: further evidence for assignment of the locus to Xq13–Xq21 Marianne SchwartzT. RosenbergL. U. Lamm Original Investigations Pages: 449 - 452
Cell culture studies on neurofibromatosis (von Recklinghausen) Winfrid KroneInge Högemann Short Communications Pages: 453 - 455
Origin of new mutations in Duchenne muscular dystrophy Laura RoncuzziAlessandra FerliniG. Romeo Short Communications Pages: 456 - 460
Mid-trimester ultrasonographic diagnosis of early manifesting “adult” form of polycystic kidney disease J. P. FrynsK. VandenbergheF. Moerman Letters to the Editors Pages: 461 - 461