A new familial syndrome with impaired function of three related peptide growth factors H. -J. HoepffnerM. DreyerH. W. Rüdiger Original Investigations Pages: 209 - 216
Impairment of capping in lymphoblastoid cell lines of Duchenne patients indicates an intrinsic cellular defect O. R. BaricordiA. SensiE. Gandini Original Investigations Pages: 217 - 219
Different haplotypes for cystic fibrosis-linked DNA polymorphisms in Polish and Dutch populations Dorota MaciejkoJerzy BalDicky Halley Original Investigations Pages: 220 - 222
Probe walking: development of novel probes for DNA fingerprinting Keiko WashioShogo MisawaShintaroh Ueda Original Investigations Pages: 223 - 226
Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction Wenda L. GreerMelanie M. MahtaniKatherine A. Siminovitch Original Investigations Pages: 227 - 230
Somatic pairing of chromosome 1 centromeres in interphase nuclei of human cerebellum E. P. J. ArnoldusA. C. B. PetersM. van der Ploeg Original Investigations Pages: 231 - 234
Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal aysnapsis R. S. IkonenM. LindlöfA. de la Chapelle Original Investigations Pages: 235 - 238
Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome) Susanne SchnittgerChristiane HöfersIngo Hansmann Original Investigations Pages: 239 - 244
Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy Hubertus J. M. SmeetsHan G. BrunnerBé Wieringa Original Investigations Pages: 245 - 251
Human BF*F-subtypes: segregation analysis with inclusion of MHC haplotypes G. GeserickG. MauffHelga Schröder Original Investigations Pages: 252 - 256
Population bottlenecks in Polynesia revealed by minisatellites J. FlintA. J. BoyceJ. B. Clegg Original Investigations Pages: 257 - 263
Sublocalization of von Willebrand factor pseudogene to 22q11.22–q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation P. PatracchiniE. CalzolariF. Bernardi Original Investigations Pages: 264 - 266
Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia R. W. HendriksE. J. B. M. MensinkR. K. B. Schuurman Original Investigations Pages: 267 - 270
Genotoxic effect of benzene hexachloride in cultured human lymphocytes D. S. RupaP. P. ReddyO. S. Reddi Original Investigations Pages: 271 - 273
Correlation between chromosomal breakpoint positions and synaptic behaviour in human males heterozygous for a pericentric inversion A. de PerdigoO. Gabriel-RobezY. Rumpler Original Investigations Pages: 274 - 276
Chromosome abnormalities in early pregnancy analyzed by direct chromosome preparation of chorionic villi Xianting ZhouHoushun TongYingqi Cui Original Investigations Pages: 277 - 279
Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping Henk MeijerGuus J. H. HamersJoep P. M. Geraedts Original Investigations Pages: 280 - 286
Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis David H. LockwoodAnna FarrierJudith Allanson Short Communications Pages: 287 - 288
Regional chromosomal assignment of the human glucocorticoid receptor gene to 5q31 A. TheriaultE. BoydJ. M. Connor Short Communications Pages: 289 - 291
X-linked megalocornea: close linkage to DXS87 and DXS94 J. D. ChenD. MackeyM. J. Denton Short Communications Pages: 292 - 294
Expression of the human ETS-2 oncogene in normal fetal tissues and in the brain of a fetus with trisomy 21 M. BafficoL. PerroniP. Scartezzini Short Communications Pages: 295 - 296
Assignment of the gene(s) involved in the expression of the proliferation-related Ki-67 antigen to human chromosome 10 D. M. SchonkH. J. H. KuijpersF. C. S. Ramaekers Short Communications Pages: 297 - 299
Trisomy 18 in monozygotic twins A. F. P. MulderJ. van EyckJ. W. Wladimiroff Clinical Case Report Pages: 300 - 301
Deletion 3q27→3qter in an infant with mild dysmorphism, parietal meningocele, and neonatal miliaria rubra-like lesions Irma JokiahoArmi SaloJaana Pihkala Case Observed Pages: 302 - 304
Detection of a rare allele with the pMP6d-9/MspI RFLP near the cystic fibrosis locus V. NunesT. CasalsX. Estivill DNA Variants Pages: 305 - 306