One gene, several messages. From multifunctional proteins to endogenous opiates J. FrézalA. MunnichG. Mitchell Review Articles Pages: 311 - 314
Decreased oxygen supply enhances growth in culture of human mid-trimester amniotic fluid cells M. BrackertzM. KubbiesD. Salk Original Investigations Pages: 334 - 338
Use of repetitive DNA for diagnosis of chromosomal rearrangements R. D. BurkJudith StambergK. D. Smith Original Investigations Pages: 339 - 342
The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families L. IseliusJ. LindstenO. Zuffardi Original Investigations Pages: 343 - 355
Prader-Willi syndrome and chromosome 15 J. F. MatteiM. G. MatteiF. Giraud Original Investigations Pages: 356 - 362
Silver staining of nucleolus organizer regions during human spermatogenesis M. SchmidHj. MüllerW. Engel Original Investigations Pages: 363 - 370
Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome T. TønnesenF. GüttlerC. Lykkelund Original Investigations Pages: 371 - 375
Hb M Milwaukee: Direct detection of the β-globin gene mutation in three generations of an afflicted family Renate OehmeElisabeth KohneJ. Horst Original Investigations Pages: 376 - 379
Genetic studies of an apoA-I lipoprotein variant O. SchamaunB. OlaisenP. Teisberg Original Investigations Pages: 380 - 383
Unusual response to bifunctional alkylating agents in a case of Fanconi anaemia M. L. KweeE. H. A. PollH. Joenje Original Investigations Pages: 384 - 387
Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment M. FraccaroO. ZuffardiV. Vigi Original Investigations Pages: 388 - 394
Red cell glyoxalase I polymorphism in Basque and Castilian populations M. Martínez de PancorboMaría IsusquizaC. Ma Lostao Original Investigations Pages: 395 - 397
Prevalence of primary adult lactose malabsorption in Hungary A. CzeizelG. FlatzSibylle D. Flatz Original Investigations Pages: 398 - 401
Ineffectivity of accessory bisatellited marker chromosomes in inducing meiotic nondisjunction P. SteinbachM. Djalali Short Communications Pages: 402 - 403
Reliability of the Tønnesen technique for the identification of Hunter carriers L. PetruschkaG. MachillA. Knapp Short Communications Pages: 404 - 406
Familial insulin-resistant diabetes secondary to an affinity defect of the insulin receptor H. W. RüdigerM. DreyerH. Bartelheimer Clinical Case Reports Pages: 407 - 411
De novo inversion 1, in amniotic, fluid cell cultures Maria Stührenberg Cases Observed Pages: 412 - 412
