Modification in publication of articles dealing with genetic polymorphisms Editorial Pages: 359 - 359
Genetic changes in mammalian cells reminiscent of an SOS response P. HerrlichU. MallickH. J. Rahmsdorf Review Articles Pages: 360 - 368
Three new phenotypes of human red cell acid phosphatase: ACP1FA, ACP1GA, and ACP1GB M. S. NelsonE. A. SmithE. G. Reisner Original Investigations Pages: 369 - 371
A re-examination of the case for homology between the X and Y chromosomes of mouse and man Terry Ashley Original Investigations Pages: 372 - 377
Population genetics of the vitamin D binding protein (GC) subtypes in the Asian-Pacific area: Description of new alleles at the GC locus M. I. KambohP. R. RanfordR. L. Kirk Original Investigations Pages: 378 - 384
Telomeric association of chromosomes in B-cell lymphoid leukemia Peter H. FitzgeraldChristine M. Morris Original Investigations Pages: 385 - 390
Heterochromatin and nucleolus organizer regions in cells of patients with malignant and premalignant lymphatic diseases Bernt SchulzeCornelia GolinskiChrista Fonatsch Original Investigations Pages: 391 - 395
A gene regulating the time dependence of α-l-fucosidase concentration is closely linked with the structural gene in man B. TümmlerM. DuthieJ. R. Riordan Original Investigations Pages: 396 - 399
On the development of a standard two-dimensional polypeptide map of the human X chromosome Ulrich MüllerIon Voiculescu Original Investigations Pages: 400 - 405
The gene for coagulation factor XIII a subunit (F13A) is distal to HLA on chromosome 6 P. G. BoardM. ReidS. Serjeantson Original Investigations Pages: 406 - 408
A new X-linked dysplasia gigantism syndrome: Identical with the Simpson dysplasia syndrome? A. BehmelE. PlöchlW. Rosenkranz Original Investigations Pages: 409 - 413
Diagnosis of infantile and juvenile forms of GM2 gangliosidosis variant 0. residual activities toward natural and different synthetic substrates H. -J. KytziaU. HinrichsK. Sandhoff Original Investigations Pages: 414 - 418
Transmission of the marker X syndrome trait by unaffected males: Conclusions from studies of large families Ursula Froster-IskeniusAnnegret SchulzeE. Schwinger Original Investigations Pages: 419 - 427
Restriction fragment length polymorphisms at the human parathyroid hormone gene locus Jörg SchmidtkeBettina PapeHubert Mayer Original Investigations Pages: 428 - 431
Gaucher disease: The effects of phosphatidylserine on glucocerebrosidase from normal and Gaucher fibroblasts Francis Y. M. Choy Original Investigations Pages: 432 - 436
C3 polymorphism, HLA and chronic renal failure in Spaniards J. R. RegueiroA. Arnaiz-Villena Original Investigations Pages: 437 - 440
Techniques for estimating genetic admixture and applications to the problem of the origin of the Icelanders and the Ashkenazi Jews Ellen M. Wijsman Original Investigations Pages: 441 - 448
Further study on a BF silent allele Katsushi TokunagaKeiichi OmotoEtsuko Maruya Short Communications Pages: 449 - 451
Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): Linkage studies in a large Dutch family Frederic H. MenkoOlav L. M. BijvoetLodewijk N. Went Short Communications Pages: 452 - 454
Del11p13/nephroblastoma without aniridia Catherine TurleauJ. de GrouchyClaudine Junien Clinical Case Reports Pages: 455 - 456
X-Y translocation. A case report I. T. CameronKarin E. BucktonD. T. Baird Clinical Case Reports Pages: 457 - 459
X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers B. Kaladhar ReddyT. E. AnandavalliO. S. Reddi Clinical Case Reports Pages: 460 - 462
