A possible new locus of alkaline phosphatase expressed in human testis J. L. MillánA. ErikssonT. Stigbrand Original Investigations Pages: 293 - 295
Epistatic association and linkage analysis in human families Jurg OttCatherine T. Falk Original Investigations Pages: 296 - 300
Specfic staining of 9h in human somatic interphase cells by D 287/170 Niels Tommerup Original Investigations Pages: 301 - 304
Sister chromatid exchanges and structural chromosome aberrations in relation to age and sex Karin HednerBenkt HögstedtFelix Mitelman Original Investigations Pages: 305 - 309
Quantitative studies on the arrangement of human metaphase chromosomes. IX. Arrangement of chromosomes with and without spindle apparatus C. WollenbergM. P. KiefaberK. D. Zang Original Investigations Pages: 310 - 315
Trisomy 21: Origin of non-disjunction J. del MazoAmalia Pérez CastilloJ. A. Abrisqueta Original Investigations Pages: 316 - 320
Analysis of heterogeneity in Fanconi's anemia patients of different ethnic origin Sabine ZakrzewskiK. Sperling Original Investigations Pages: 321 - 323
Extracentromeric connections between sister chromatids demonstrated in human chromosomes induced to condense asymmetrically V. J. GoyanesJ. Méndez Original Investigations Pages: 324 - 326
The cell cycle of lymphocytes in Fanconi anemia B. DutrillauxA. AuriasMarguerite Prieur Original Investigations Pages: 327 - 332
Biochemical and genetic characterization of the lowell variant. A new phenotype of 6-phosphogluconate dehydrogenase M. S. Nelson Original Investigations Pages: 333 - 336
Assignment of the structural gene coding for albumin to human chromosome 4 Fa-Ten KaoJ. W. HawkinsA. Dugaiczyk Original Investigations Pages: 337 - 341
Patterns of exchange induced by mitomycin C in C-bands of human chromosomes. I. Relationship to C-band size in chromosomes 1, 9, and 16 J. L. JosephJ. M. BraschD. R. Smyth Original Investigations Pages: 342 - 345
Patterns of exchange induced by mitomycin C in C-bands of human chromosomes. II. High frequency of Y-Y exchange in XYY cells J. L. JosephJ. M. BraschD. R. Smyth Original Investigations Pages: 346 - 348
Apolipoprotein A-IV polymorphism in man Hans-Jürgen MenzelMichael Peter KövaryGerd Assmann Original Investigations Pages: 349 - 352
Expression of fra(X)(q28) is Suppressed in man-mouse hybrid cells Rolf-Dieter WegnerBettina GeiselerKarl Sperling Short Communications Pages: 353 - 354
Karyotyping chromosomes by electron microscopy. II. A method for the sequential examination of spread and banded metaphases by light and electron microscopy V. J. GoyanesJ. Méndez Short Communications Pages: 355 - 357
Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34) R. A. PfeifferR. OttP. Alexandre Clinical Case Reports Pages: 358 - 360
Mirror image duplications of chromosome 21. Three new cases and discussion of the mechanisms of origin R. A. PfeifferJ. Loidl Clinical Case Reports Pages: 361 - 363
Ring 18 mosaicism in identical twins akira HataYasuyuki SuzukiYoshikazu Kuroki Clinical Case Reports Pages: 364 - 367
A new glucose-6-phosphate dehydrogenase variant (G6PD Nagano) associated with congenital hemolytic anemia K. TakahashiH. FujiiS. Miwa Clinical Case Reports Pages: 368 - 370
Tetraploid conceptus with three paternal contributions D. M. SheppardRosemary A. FisherSusan Povey Clinical Case Reports Pages: 371 - 374
Crossing-over during human spermatogenesis visualized cytologically I. HansmannM. GeislerT. Grimm Clinical Case Reports Pages: 375 - 377
Partial trisomy for the long arm of chromosome 7. Case report and review M. A. NovalesC. Fernandez-NovoaH. Galera Clinical Case Reports Pages: 378 - 381
Four patients including two sisters with the acrocallosal syndrome (Agenesis of the corpus callosum in combination with preaxial hexadactyly) A. Schinzel Cases Observed Pages: 382 - 382
A syndrome of midface retraction, multiple radiological anomalies, renal malformations and hypertrichosis A. Schinzel Cases Observed Pages: 382 - 382
