The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuria Jadwiga JaruzelskaKaren Friis HenriksenRyszard Slomski Original Investigations Pages: 247 - 250
An assay for the rapid detection of the arylsulfatase A pseudodeficiency allele facilitates diagnosis and genetic counseling for metachromatic leukodystrophy Volkmar Gieselmann Original Investigations Pages: 251 - 255
Fragile sites and chromosome instability: the distribution of breaks induced by cis-diamine-clichloro-platinum (II) in Fanconi anemia lymphocyte cultures B. PorfirioD. SmeetsB. Dallapiccola Original Investigations Pages: 256 - 260
Identification of a break-prone structure in the 9q1 heterochromatic region Zissis MamurisAlain AuriasBernard Dutrillaux Original Investigations Pages: 261 - 264
No evidence of linkage between the locus for autosomal dominant retinitis pigmentosa and D3S47 (C17) in three Australian families Jacqueline B. JiménezChristine SamannsMichael J. Denton Original Investigations Pages: 265 - 267
Assignment of the human CD9 gene to chromosome 12 (region P13) by use of human specific DNA probes P. BenoitM. S. GrossNguyen Van Cong Original Investigations Pages: 268 - 272
Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism Kerstin WielandDavid S. MillarDavid N. Cooper Original Investigations Pages: 273 - 278
Synaptonemal complex analysis in a human male carrier of a 4;6 translocation: heterosynapsis without previous homosynapsis A. de PerdigoO. Gabriel-RobezY. Rumpler Original Investigations Pages: 279 - 282
Frequency and distribution of aneuploidy in human female gametes Franck Pellestor Original Investigations Pages: 283 - 288
A pooling strategy for heterozygote screening of the ΔF508 cystic fibrosis mutation Christoph GilleKlaus GradeCharles Coutelle Original Investigations Pages: 289 - 291
Molecular analysis of PKU haplotypes in the population of southern Poland Marta ZygulskaAntonin EigelJürgen Horst Original Investigations Pages: 292 - 294
Consanguinity sans reproche Leo P. Ten KateHans SchefferJoan G. van Lookeren Campagne Original Investigations Pages: 295 - 296
Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers A. SefianiR. M'radM. C. Hors-Cayla Original Investigations Pages: 297 - 299
Autosomal dominant transmission of the NAME syndrome (nevi, atrial myxoma, mucinosis of the skin and endocrine overactivity) R. J. J. KoopmanR. Happle Original Investigations Pages: 300 - 304
PAH 399 GTA(Val)→GTT(Val), a new silent mutation found in the Chinese Shu-zhen HuangZhao-rui RenSavio L. C. Woo Short Communications Pages: 305 - 306
TaqI reveals two independent alphoid polymorphisms on human chromosomes 13 and 21 B. MarçaisA. GérardG. Roizès Short Communications Pages: 307 - 310
Structural organization and polymorphism of the alpha satellite DNA sequences of chromosomes 13 and 21 as revealed by pulse field gel electrophoresis B. MarçaisM. BellisG. Roizès Short Communications Pages: 311 - 316
No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers Katrin KauschClemens R. MüllerKlaus Zerres Short Communications Pages: 317 - 318
Hemoglobin Stanleyville II (α78 Asn→Lys) is associated with a 3.7-kb α-globin gene deletion F. F. CostaM. F. SonatiM. A. Zago Short Communications Pages: 319 - 320
Allelic somatic mutations may explain vascular twin nevi Rudolf Happle Short Communications Pages: 321 - 322
Apolipoprotein A-IV protein polymorphism: frequency and effects on lipids, lipoproteins, and apolipoproteins among Mexican-Americans in Starr County, Texas Craig L. HanisTommy C. DouglasDavid Hewett-Emmett Short Communications Pages: 323 - 325
Type III hyperlipoproteinemia in a patient with idiopathic hemochromatosis G. FeussnerR. Ziegler Clinical Case Report Pages: 326 - 328
Frequency of the cystic fibrosis mutation ΔF508 in Poland J. BalD. MaciejkoJ. Reiss Letter to the Editors Pages: 329 - 329
