1. Mapping eight new polymorphisms in 11q13 in the vicinity of multiple endocrine neoplasia type 1: identification of a new distal recombinant

   • Carissa M. Smith
   • Samuel A. Wells
   • Daniela S. Gerhard

   Review Article Pages: 377 - 387

2. Effects of the mutant von Willebrand factor gene in von Willebrand disease

   • Zhiping Zhang
   • Monica Lindstedt
   • Maria Anvret

   Original Investigation Pages: 388 - 394

3. 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 Kainulainen
   • Heikki Swan
   • Kimmo Kontula

   Original Investigation Pages: 395 - 400

4. Two novel frameshift mutations in the low density lipoprotein receptor gene generated by endogenous sequence-directed mechanisms

   • Armand V. Peeters
   • Luc F. Van Gaal
   • Maritha J. Kotze

   Original Investigation Pages: 401 - 406

5. Genetic mapping of Xp22.12–p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL)

   • Solange Heuertz
   • Asmae Smahi
   • Marie-Claude Hors-Cayla

   Original Investigation Pages: 407 - 410

6. ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome

   • Donald C. Brown
   • Elizabeth Grace
   • Patricia M. Ellis

   Original Investigation Pages: 411 - 416

7. A common β hexosaminidase gene mutation in adult Sandhoff disease patients

   • Macarena Gomez-Lira
   • Antonella Sangalli
   • Alessandro Salviati

   Original Investigation Pages: 417 - 422

8. Mapping dystrophin gene recombinants in Greek DMD/BMD families: low recombination frequencies in the STR region

   • Lina Florentin
   • Chrysanthy Bili
   • Catherine Metaxotou

   Original Investigation Pages: 423 - 426

9. Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2Rγ chain gene by single-strand conformation polymorphism analysis

   • Paula A. Clark
   • Tracy Lester
   • Christine Kinnon

   Original Investigation Pages: 427 - 432

10. Tumor necrosis factor alpha (TNF-α) gene polymorphism in alopecia areata

    • Gillian M. P. Galbraith
    • Janardan P. Pandey

    Original Investigation Pages: 433 - 436

11. Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3

    • Jon Thor Bergthorsson
    • Gudny Eiriksdottir
    • Sigurdur Ingvarsson

    Original Investigation Pages: 437 - 443

12. Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome

    • A. Mari
    • F. Amati
    • B. Dallapiccola

    Original Investigation Pages: 444 - 448

13. Improved carrier testing for multiple endocrine neoplasia, type 1, using new microsatellite-type DNA markers

    • Soili Kytölä
    • Jaakko Leisti
    • Pasi Salmela

    Original Investigation Pages: 449 - 453

14. Nature and frequency of mutations in the argininosuccinate synthetase gene that cause classical citrullinemia

    • Keiko Kobayashi
    • Hiroshige Kakinoki
    • Takeyori Saheki

    Original Investigation Pages: 454 - 463

15. Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion

    • Attila Tar
    • János Sólyom
    • Ken McElreavey

    Original Investigation Pages: 464 - 468

16. A novel coding exon of the human adenomatous polyposis coli gene

    • Zora Šuleková
    • Wolfgang G. Ballhausen

    Short Communication Pages: 469 - 471

17. Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU families

    • Libor Kozák
    • Viera Kuhrová
    • Anna Pijáčková

    Short Communication Pages: 472 - 476

18. Subregional mapping of the human gonadotropin-releasing hormone receptor (GnRH-R) gene to 4q between the markers D4S392 and D4S409

    • M. L. Kottler
    • F. Lorenzo
    • R. Counis

    Short Communication Pages: 477 - 480

19. Precise localization of the human thyroxine-binding globulin gene to chromosome Xq22.2 by fluorescence in situ hybridization

    • Yuichi Mori
    • Yoshitaka Miura
    • Kozaki Takazumi

    Short Communication Pages: 481 - 482

20. Role of genetic factors in bronchial cancer. Based upon a case of anaplastic lung carcinoma in identical twins

    • J. M. Nores
    • J. F. Dalayeun
    • J. M. Remy

    Clinical Case Report Pages: 483 - 484

21. Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene?

    • Joan E. Pellegrino
    • Rhonda E. Schnur
    • Nancy B. Spinner

    Clinical Case Report Pages: 485 - 489

22. A region of primer binding variation at the D6S265 locus associated with HLA-A25 and HLA-A26 antigens

    • Wendy Pyper
    • Michael Burt
    • Elizabeth Jazwinska

    DNA Variants Pages: 490 - 492

23. Detection of a C-insertion polymorphism within the human tumor necrosis factor alpha (TNFA) gene

    • Brigitta M. N. Brinkman
    • Eric L. Kaijzel
    • Cornelis L. Verweij

    DNA Variants Pages: 493 - 493

24. An intragenic TaqI polymorphism in the faciogenital dysplasia (FGD1) locus, the gene responsible for Aarskog syndrome

    • N. German Pasteris
    • Jerome L. Gorski

    DNA Variants Pages: 494 - 494

25. Polymorphic (AAT)n trinucleotide repeats derived from a human brain cDNA library

    • Russell L. Margolis
    • Theresa S. Breschel
    • Christopher A. Ross

    DNA Variants Pages: 495 - 496

26. Dinucleotide repeat polymorphism at the D5S99 locus on chromosome 5q33–34

    • Ilse M. Groenewald
    • Louise Warnich
    • Andries E. Retief

    DNA Variants Pages: 497 - 499

27. The importance of clinical documentation in genetic studies of male infertility

    • Dieter Meschede
    • Eberhard Nieschlag
    • Jürgen Horst

    Letter to the Editors Pages: 500 - 501

28. Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4)

    • Rajendra Kumar-Singh
    • Daniel G. Bradley
    • Peter Humphries

    Erratum Pages: 502 - 502