Mapping eight new polymorphisms in 11q13 in the vicinity of multiple endocrine neoplasia type 1: identification of a new distal recombinant Carissa M. SmithSamuel A. WellsDaniela S. Gerhard Review Article Pages: 377 - 387
Effects of the mutant von Willebrand factor gene in von Willebrand disease Zhiping ZhangMonica LindstedtMaria Anvret Original Investigation Pages: 388 - 394
Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant gene Katariina KainulainenHeikki SwanKimmo Kontula Original Investigation Pages: 395 - 400
Two novel frameshift mutations in the low density lipoprotein receptor gene generated by endogenous sequence-directed mechanisms Armand V. PeetersLuc F. Van GaalMaritha J. Kotze Original Investigation Pages: 401 - 406
Genetic mapping of Xp22.12–p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL) Solange HeuertzAsmae SmahiMarie-Claude Hors-Cayla Original Investigation Pages: 407 - 410
ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome Donald C. BrownElizabeth GracePatricia M. Ellis Original Investigation Pages: 411 - 416
A common β hexosaminidase gene mutation in adult Sandhoff disease patients Macarena Gomez-LiraAntonella SangalliAlessandro Salviati Original Investigation Pages: 417 - 422
Mapping dystrophin gene recombinants in Greek DMD/BMD families: low recombination frequencies in the STR region Lina FlorentinChrysanthy BiliCatherine Metaxotou Original Investigation Pages: 423 - 426
Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2Rγ chain gene by single-strand conformation polymorphism analysis Paula A. ClarkTracy LesterChristine Kinnon Original Investigation Pages: 427 - 432
Tumor necrosis factor alpha (TNF-α) gene polymorphism in alopecia areata Gillian M. P. GalbraithJanardan P. Pandey Original Investigation Pages: 433 - 436
Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3 Jon Thor BergthorssonGudny EiriksdottirSigurdur Ingvarsson Original Investigation Pages: 437 - 443
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome A. MariF. AmatiB. Dallapiccola Original Investigation Pages: 444 - 448
Improved carrier testing for multiple endocrine neoplasia, type 1, using new microsatellite-type DNA markers Soili KytöläJaakko LeistiPasi Salmela Original Investigation Pages: 449 - 453
Nature and frequency of mutations in the argininosuccinate synthetase gene that cause classical citrullinemia Keiko KobayashiHiroshige KakinokiTakeyori Saheki Original Investigation Pages: 454 - 463
Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion Attila TarJános SólyomKen McElreavey Original Investigation Pages: 464 - 468
A novel coding exon of the human adenomatous polyposis coli gene Zora ŠulekováWolfgang G. Ballhausen Short Communication Pages: 469 - 471
Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU families Libor KozákViera KuhrováAnna Pijáčková Short Communication Pages: 472 - 476
Subregional mapping of the human gonadotropin-releasing hormone receptor (GnRH-R) gene to 4q between the markers D4S392 and D4S409 M. L. KottlerF. LorenzoR. Counis Short Communication Pages: 477 - 480
Precise localization of the human thyroxine-binding globulin gene to chromosome Xq22.2 by fluorescence in situ hybridization Yuichi MoriYoshitaka MiuraKozaki Takazumi Short Communication Pages: 481 - 482
Role of genetic factors in bronchial cancer. Based upon a case of anaplastic lung carcinoma in identical twins J. M. NoresJ. F. DalayeunJ. M. Remy Clinical Case Report Pages: 483 - 484
Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene? Joan E. PellegrinoRhonda E. SchnurNancy B. Spinner Clinical Case Report Pages: 485 - 489
A region of primer binding variation at the D6S265 locus associated with HLA-A25 and HLA-A26 antigens Wendy PyperMichael BurtElizabeth Jazwinska DNA Variants Pages: 490 - 492
Detection of a C-insertion polymorphism within the human tumor necrosis factor alpha (TNFA) gene Brigitta M. N. BrinkmanEric L. KaijzelCornelis L. Verweij DNA Variants Pages: 493 - 493
An intragenic TaqI polymorphism in the faciogenital dysplasia (FGD1) locus, the gene responsible for Aarskog syndrome N. German PasterisJerome L. Gorski DNA Variants Pages: 494 - 494
Polymorphic (AAT)n trinucleotide repeats derived from a human brain cDNA library Russell L. MargolisTheresa S. BreschelChristopher A. Ross DNA Variants Pages: 495 - 496
Dinucleotide repeat polymorphism at the D5S99 locus on chromosome 5q33–34 Ilse M. GroenewaldLouise WarnichAndries E. Retief DNA Variants Pages: 497 - 499
The importance of clinical documentation in genetic studies of male infertility Dieter MeschedeEberhard NieschlagJürgen Horst Letter to the Editors Pages: 500 - 501
Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4) Rajendra Kumar-SinghDaniel G. BradleyPeter Humphries Erratum Pages: 502 - 502