A human UPD-GalNAc: polypeptide, N-acetylgalactosaminyltranferase type 1 gene is located at the chromosomal region 18q12.1 Setsuo TakaiYuji HinodaM. Oshima Original investigation Pages: 293 - 294
The mapping and visual ordering of the human syndecan-1 and N-myc genes near the telomeric region of chromosome 2p Jaakko KaukonenLeena Alanen-KurkiA. Palotie Original investigation Pages: 295 - 297
An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses Laurence Legeai-MalletPatricia Margaritte-JeanninFrançoise Clerget-Darpoux Original investigation Pages: 298 - 302
Close physical linkage of the genes encoding the pNR-2/pS2 protein and human spasmolytic protein (hSP) F. E. B. MayBruce R. Westley Original investigation Pages: 303 - 307
Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique R. WillemsenArie SmitsB. A. Oostra Original investigation Pages: 308 - 311
DNA multiallelic systems reveal gene/longevity associations not detected by diallelic systems. The APOB locus G. De BenedictisE. FalconeC. Franceschi Original investigation Pages: 312 - 318
Laryngeal and oropharyngeal cancer, and alcohol dehydrogenase 3 and glutathione S-transferase M1 polymorphisms C. CoutelleP. J. WardA. Cassaigne Original investigation Pages: 319 - 325
Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region J. DeckertMarkus M. NöthenPeter Propping Original investigation Pages: 326 - 328
Isolation of a cDNA encoding the human homolog of COX17, a yeast gene essential for mitochondrial copper recruitment Ravi AmaravadiD. Moira GlerumA. Tzagoloff Original investigation Pages: 329 - 333
The human homolog of the rodent immediate early response genes, PC4 and TIS7, resides in the lung cancer tumor suppressor gene region on chromosome 3p21 F. LatifFuh-Mei DuhMichael I. Lerman Original investigation Pages: 334 - 341
Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism F. FarneboBin Tean TehCatharina Larsson Original investigation Pages: 342 - 349
A C57BL/KsJ mouse model of Niemann-Pick disease (spm) belongs to the same complementation group as the major childhood type of Niemann-Pick disease type C S. AkaboshiTamami YanoKenzo Takeshita Original investigation Pages: 350 - 353
Southern analysis for detection of CAG repeat expansions associated with dentatorubral pallidoluysian atrophy R. L. AlfordR. L. MargolisC. S. Richards Original investigation Pages: 354 - 356
Interethnic polymorphism of EWS intron 6: genome plasticity mediated by Alu retroposition and recombination Jessica Zucman-RossiMark A. BatzerGilles Thomas Original investigation Pages: 357 - 363
Rapid detection of trisomy 21 by homologous gene quantitative PCR (HGQ-PCR) Hsien-Hsiung LeeJan-Gowth ChangHeung-Tat Ng Original investigation Pages: 364 - 367
Genomic organization and chromosomal localization of the human casein gene family Y. FujiwaraM. MiwaM. Ueda Original investigation Pages: 368 - 373
High-resolution comparative hybridization to combed DNA fibers Jürgen KrausRuthild G. WeberThomas Cremer Original investigation Pages: 374 - 380
Molecular basis of α-thalassemia in Sicily Marco FicheraAngela SpallettaA. Ragusa Original investigation Pages: 381 - 386
Cloning a new human gene from chromosome 21q22.3 encoding a glutamic acid-rich protein expressed in heart and skeletal muscle P. ScartezziniAliana EgeoAlberto Rasore-Quartino Original investigation Pages: 387 - 392
Human orosomucoid polymorphism: molecular basis of the three common ORM1 alleles, ORM1*F1, ORM1*F2, and ORM1*S I. YuasaKazuo UmetsuYoshito Irizawa Original investigation Pages: 393 - 398
Coding versus intron variability: extremely polymorphic HLA-DRB1 exons are flanked by specific composite microsatellites, even in distant populations C. EpplenEduardo J. M. SantosJörg T. Epplen Original investigation Pages: 399 - 406
Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35 142 sperm nuclei from two 47,XYY males E. ChevretS. RousseauxB. Sèle Rapid communication Pages: 407 - 412
Increased incidence of disomic sperm nuclei in a 47,XYY male assessed by fluorescent in situ hybridization (FISH) Joan BlancoCarmen RubioF. Vidal Rapid communication Pages: 413 - 416
Suggestive evidence for linkage of schizophrenia to markers on chromosome 13 in Caucasian but not Oriental populations M.-W. LinP. ShamJohn F. Powell Rapid communication Pages: 417 - 420