Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs Han-Xiang DengKyohko AbeNorio Niikawa Original Investigations Pages: 541 - 544
Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli Niels GregersenBrage S. AndresenSandro Ghisla Original Investigations Pages: 545 - 551
Ovarian dysgenesis in individuals with chromosomal abnormalities Christopher CunniffKenneth Lyons JonesKurt Benirschke Original Investigations Pages: 552 - 556
Polymorphism in a ferritin H gene from chromosome 6p Elisabetta ZapponeIsabelle DugastJim Drysdale Original Investigations Pages: 557 - 561
Cytogenetic and molecular characterization of a newly established neuroblastoma cell line LS Günter RudolphKarin Schilbach-StückleHorst Hameister Original Investigations Pages: 562 - 566
Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genes Michael I. LermanFarida LatifBerton Zbar Original Investigations Pages: 567 - 577
DNA polymorphism haplotypes of the human lipoprotein lipase gene: possible association with high density lipoprotein levels Camilla HeizmannTodd KirchgessnerAldons J. Lusis Original Investigations Pages: 578 - 584
Two human genes encoding zinc finger proteins, ZNF12 (KOX 3) and ZNF 26 (KOX 20), map to chromosomes 7p22-p21 and 12q24.33, respectively P. SeiteK. HuebnerH. J. Thiesen Original Investigations Pages: 585 - 590
The linkage of Hb Valletta [α2β287(F3)Thr→Pro] and Hb F-Malta-I [α2 Gγ2117(G19)His→Arg] in the Maltese population Ferdane KutlarAlexander E. FeliceTitus H. J. Huisman Original Investigations Pages: 591 - 594
A marked drop in the incidence of the null allele of the B gene of the fourth component of complement (C4B*Q0) in elderly subjects: C4B*Q0 as a probable negative selection factor for survival Judit KramerTamás FülöpGeorge Füst Original Investigations Pages: 595 - 598
Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region Tiina AlitaloTorben A. KruseAlbert de la Chapelle Original Investigations Pages: 599 - 603
Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations N. ArchidiaconoM. LeroneG. Romeo Original Investigations Pages: 604 - 606
Effects of the apolipoprotein(a) size polymorphism on the lipoprotein(a) concentration in 7 ethnic groups C. SandholzerD. M. HallmanG. Utermann Original Investigations Pages: 607 - 614
A method for transforming lymphocytes from very small blood volumes suitable for paediatric samples J. ElliottM. B. Coulter-MackieS. M. Singh Short Communications Pages: 615 - 616
Correction of the published sequence for the human proteolipid protein gene Paul J. WilkinsCynthia R. D'SouzaPeter J. Bridge Short Communications Pages: 617 - 618
Determination of the origin of nondisjunction in a 49,XXXXY male using hypervariable dinucleotide repeat sequences Tim H. -M. HuangFrank GreenbergDavid H. Ledbetter Short Communications Pages: 619 - 620
Assignment of the gene for human tenascin to the region q32–q34 of chromosome 9 Mariano RocchiNicoletta ArchidiaconoLuciano Zardi Short Communications Pages: 621 - 623
New RFLPs of the immunoglobulin switch alpha region in mesangial IgA glomerulonephritis G. KeyeuxP. NusbaumM. -P. Lefranc DNA Variants Pages: 624 - 624
A tetranucleotide repeat polymorphism in the cystic fibrosis gene P. GaspariniM. DogniniX. Estivill DNA Variants Pages: 625 - 625
