Molecular defect in human erythropoietic protoporphyria with fatal liver failure Yoshitsugu NakahashiHiroaki MiyazakiShigeru Taketani Original Investigations Pages: 303 - 306
Presymptomatic direct detection of adenomatous polyposis coli (APC) gene mutations in familial adenomatous polyposis Gloria M. PetersenClair FrancomanoYusuke Nakamura Original Investigations Pages: 307 - 311
Support for founder effect for two lipoprotein lipase (LPL) gene mutations in French Canadians by analysis of GT microsatellites flanking the LPL gene Stephen WoodMichael SchertzerYuanhong Ma Original Investigations Pages: 312 - 316
Immunophenotyping of mitotic cells from long-term cultures of chorionic villi Nadja ZimmerElisabeth GöttertWolfram Henn Original Investigations Pages: 317 - 320
Single-strand conformational polymorphism and direct sequencing applied to carrier testing in families with ornithine transcarbamylase deficiency Michael Y. TsaiRobert A. HolzknechtMendel Tuchman Original Investigations Pages: 321 - 325
HLA-A/B haplotye frequencies among U.S. Hispanic and African-American populations Lloyd C. OsborneJames M. Mason Original Investigations Pages: 326 - 332
Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq Barbara BardoniGiovanna FloridiaGiovanna Camerino Original Investigations Pages: 333 - 338
The two locus control of Leber hereditary optic neurophathy and a high penetrance in Japanese pedigrees Makoto NakamuraYoshisada FujiwaraMisao Yamamoto Original Investigations Pages: 339 - 341
Patterns of deletions of the dystrophin gene in different European populations Gian Antonio DanieliFederico MioniTiemo Grimm Original Investigations Pages: 342 - 346
FFU complex: an analysis of 491 cases Widukind LenzMarta ZygulskaJürgen Horst Original Investigations Pages: 347 - 356
Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q E. C. M. MarimanS. E. C. van BeersumH. H. Ropers Original Investigations Pages: 357 - 361
Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkage Astrid LunkesSuzana GispertGeorg Auburger Original Investigations Pages: 362 - 366
Autosomal recessive transmission of hemophilia A due to a von Willebrand factor mutation Robert J. WiseBruce M. EwensteinRobert I. Handin Original Investigations Pages: 367 - 372
Excess of multifocal tumors in nephroblastoma: implications for mechanisms of tumor development and genetic counseling Catherine Bonaïti-PelliéAgnès ChompretJan F. M. Delemarre Original Investigations Pages: 373 - 376
A parental combination analysis for ABO-HP interaction in a Bengali population Arup Ratan Bandyopadhyay Original Investigations Pages: 377 - 379
Elevated frequency of an ETS-1 restriction fragment polymorphism in chronic B-cell leukaemia Peter E. CrossenMary J. Morrison Short Communications Pages: 380 - 382
Human zinc finger gene ZNF23 (Kox16) maps to a zinc finger gene cluster on chromosome 16q22, and ZNF32 (Kox30) to chromosome region 10q23-–q24 L. A. CannizzaroM. M. AronsonH. J. Thiesen Short Communications Pages: 383 - 385
Focal epithelial hyperplasia: human-papillomavirus-induced disease with a genetic predisposition in a Venezuelan family Gloria Premoli-De-PercocoJuan Pinto CisternasIván Galindo Short Communications Pages: 386 - 388
Molecular cytogenetic characterization of three familial cases of satellited Y chromosomes Tracy Ann WilkinsonJohn Anthony Crolla Short Communications Pages: 389 - 391
Charcot-Marie-Tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2→12 M. UpadhyayaS. H. RobertsP. S. Harper Short Communications Pages: 392 - 394
Duplication of the short arm of the X chromosome in mother and daugther Cathy M. Tuck-MullerJose E. MartinezWladimir Wertelecki Clinical Case Report Pages: 395 - 400
Human β2-glycoprotein I: molecular analysis of DNA and amino acid polymorphism Alexander SteinkassererChrista DörnerRobert B. Sim DNA Variants Pages: 401 - 402
Polymorphism in human IL-1 receptor antagonist gene intron 2 is caused by variable numbers of an 86-bp tandem repeat Joanna K. TarlowAlexandra I. F. BlakemoreGordon W. Duff DNA Variants Pages: 403 - 404
A 40-nucleotide repeat polymorphism in the human dopamine transporter gene Akira SanoKeiji KondohIkuko Kondo DNA Variants Pages: 405 - 406
A β-galactosidase gene mutation identified in both Morquio B disease and infantile GM1 gangliosidosis Y. SuzukiA. Oshima Letter to the Editors Pages: 407 - 407
