Genetic polymorphism of the apolipoprotein B gene locus influences serum LDL cholesterol level in familial hypercholesterolemia Katriina Aalto-SetäläHelena GyllingKimmo Kontula Original Investigations Pages: 305 - 307
The problem of our common mitochondrial mother J. KrügerF. Vogel Original Investigations Pages: 308 - 312
Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome Kyohko AbeTadashi KajiiNorio Niikawa Original Investigations Pages: 313 - 316
Three novel partial deletions of the low-density lipoprotein (LDL) receptor gene in familial hypercholesterolemia Kimiko YamakawaKohki TakadaHideo Hamaguchi Original Investigations Pages: 317 - 321
Apolipoprotein B amino acid 3611 substitution from arginine to glutamine creates the Ag (h/i) epitope: the polymorphism is not associated with differences in serum cholesterol and apolipoprotein B levels Chunfang XuNazeem NanjeePhilippa J. Talmud Original Investigations Pages: 322 - 326
Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndrome H. -J. LüdeckeRuth BurdiekB. Horsthemke Original Investigations Pages: 327 - 329
Fragile sites and breakpoints in constitutional rearrangements and in human sperm chromosomes C. FusterR. MiróJ. Egozcue Original Investigations Pages: 330 - 334
A case of hereditary persistence of fetal hemoglobin caused by a gene not linked to the β-globin cluster G. MartinezA. NovellettoB. Colombo Original Investigations Pages: 335 - 337
Chromosomal localization of human glutathione transferase genes of classes alpha, mu and pi M. Quamrul IslamAnton PlatzBengt Mannervik Original Investigations Pages: 338 - 342
Chromosomal characteristics of malignant lymphoma E. W. FleischmanE. L. PrigoginaD. S. Osmanov Original Investigations Pages: 343 - 348
Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq James C. SkareJohn L. SullivanAubrey Milunsky Original Investigations Pages: 349 - 353
Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37 James C. SkareHelen L. GriersonAubrey Milunsky Original Investigations Pages: 354 - 358
MASA syndrome: further clinical delineation and chromosomal localisation Robin M. WinterKay E. DaviesMark N. Patterson Original Investigations Pages: 367 - 370
The gene for human interleukin 7 (IL7) is at 8q12-13 Grant R. SutherlandElizabeth BakerMatthew A. Vadas Original Investigations Pages: 371 - 372
The predictive value of chorionic villus histology for identifying chromosomally normal and abnormal spontaneous abortions Carmen MinguillonBernd EibenIngo Hansmann Original Investigations Pages: 373 - 376
Is there a correlation between morphological and cytogenetic findings in placental tissue from early missed abortions? Helga RehderWiltrud CoerdtEberhard Schwinger Original Investigations Pages: 377 - 385
Inactivated X chromosome fold in human leukemia and related clonal disorders M. R. AvalosC. LéonardG. Tchernia Short Communications Pages: 386 - 388
Detection of β-thalassemia and hemoglobin E genes in Thai by a DNA amplification technique Pranee WinichagoonJiraporn KownkonSuthat Fucharoen Short Communications Pages: 389 - 390
Tissue-specific 45,X0/47,XY,+13 mosaicism in an 18-year-old woman B. EibenS. HansenW. Hammans Clinical Case Report Pages: 391 - 392
A new polymorphic variant of human complement factor I Ming ZhouBodil Larsen Rare Genetic Variant Register Pages: 393 - 393
Gene symbols for fragile sites: a proposal Frederick HechtLinda A. CannizzaroBarbara K. Hecht Letter to the Editors Pages: 394 - 394