1. Detection of a common mutation of the catalase gene in Japanese acatalasemic patients

   • Yosuke Kishimoto
   • Yoshinori Murakami
   • Takao Sekiya

   Original Investigations 01 March 1992 Pages: 487 - 490

2. Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells

   • Shigehiro Yajima
   • Yasuyuki Suzuki
   • Hugo W. Moser

   Original Investigations 01 March 1992 Pages: 491 - 499

3. Genetic concepts in Greek literature from the eighth to the fourth century B.C.

   • Euterpe Bazopoulou-Kyrkanidou

   Original Investigations 01 March 1992 Pages: 500 - 507

4. CFTR illegitimate transcription in lymphoid cells: quantification and applications to the investigation of pathological transcripts

   • Nuria Fonknechten
   • Jamel Chelly
   • Jean-Claude Chomel

   Original Investigations 01 March 1992 Pages: 508 - 512

5. Quantitative correlation between the residual activity of β-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease

   • P. Leinekugel
   • S. Michel
   • K. Sandhoff

   Original Investigations 01 March 1992 Pages: 513 - 523

6. Complementation of a DNA repair deficiency in six human tumor cell lines by chromosome 11

   • R. Parshad
   • F. M. Price
   • K. K. Sanford

   Original Investigations 01 March 1992 Pages: 524 - 528

7. Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians

   • Christine Bétard
   • A. M. Kessling
   • J. Davignon

   Original Investigations 01 March 1992 Pages: 529 - 536

8. Nested polymerase chain reaction on cellular DNA in plasma: a rapid method to investigate the collagen type I A2 MspI polymorphic restriction site in alcoholic patients

   • Laurence Christa
   • Jean-Pierre Zarski
   • Christian Bréchot

   Original Investigations 01 March 1992 Pages: 537 - 540

9. In situ hybridization of PCR amplified inter-Alu sequences from a hybrid cell line

   • C. Desmaze
   • J. Zucman
   • A. Aurias

   Original Investigations 01 March 1992 Pages: 541 - 544

10. CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families

    • Paul J. Sinnott
    • Chiara Livieri
    • Tom Strachan

    Original Investigations 01 March 1992 Pages: 545 - 551

11. Screening for cystic fibrosis gene mutations by multiplex DNA amplification

    • Luigi Picci
    • Franca Anglani
    • Franco Zacchello

    Original Investigations 01 March 1992 Pages: 552 - 556

12. Polymorphisms at the GLUT1 (HepG2) and GLUT4 (muscle/adipocyte) glucose transporter genes and non-insulin-dependent diabetes mellitus (NIDDM)

    • Marco G. Baroni
    • Raymond S. Oelbaum
    • David J. Galton

    Original Investigations 01 March 1992 Pages: 557 - 561

13. Genetic linkage analysis of bipolar affective disorder in an Old Order Amish pedigree

    • Adam Law
    • Charles W. Richard III
    • Richard M. Myers

    Original Investigations 01 March 1992 Pages: 562 - 568

14. The human vitronectin (complement S-protein) gene maps to the centromeric region of 17q

    • Thomas M. Fink
    • Dieter E. Jenne
    • Peter Lichter

    Original Investigations 01 March 1992 Pages: 569 - 572

15. Pseudoautosomal repeat displays higher variability in Blacks than in Caucasians

    • Gudrun A. Rappold
    • Anja Henke
    • Titus H. J. Huisman

    Original Investigations 01 March 1992 Pages: 573 - 578

16. Search for putative suppressor genes in meningioma: significance of chromosome 22

    • Günther Schneider
    • Steffi Lutz
    • Nikolaus Blin

    Original Investigations 01 March 1992 Pages: 579 - 582

17. PCR-assisted localization of the human SRPR gene

    • Nicolas Janin
    • Oliver Delattre
    • Marc Lipinski

    Short Communications 01 March 1992 Pages: 583 - 585

18. Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C gene

    • C. B. Grundy
    • S. Schulman
    • D. N. Cooper

    Short Communications 01 March 1992 Pages: 586 - 588

19. Characterization of two novel polymorphisms at the human parathyroid hormone gene locus

    • Jerald E. Mullersman
    • Jack J. Shields
    • Bratin K. Saha

    Short Communications 01 March 1992 Pages: 589 - 592

20. Localization of the human gene encoding heterogeneous nuclear RNA ribonucleoprotein G (hnRNP-G) to chromosome 6p12

    • Maryvonne Le Coniat
    • Michel Soulard
    • Roland Berger

    Short Communications 01 March 1992 Pages: 593 - 595

21. De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies

    • Yoshiharu Wakita
    • Kouji Narahara
    • Yoshiki Seino

    Clinical Case Report 01 March 1992 Pages: 596 - 598

22. Selective advantage of fra(X) heterozygotes compared with mothers of Down syndrome probands?

    • P. H. Jongbloet

    Letters to the Editors 01 March 1992 Pages: 599 - 600

23. Mothers and grandmothers of Down's syndrome patients as controls for fra(X) carriers

    • F. Vogel

    Letters to the Editors 01 March 1992 Pages: 601 - 601

24. Announcements

    Announcement 01 March 1992 Pages: 602 - 602