1. Painting of human chromosomes with probes generated from hybrid cell lines by PCR with Alu and L1 primers

   • C. Lengauer
   • H. Riethman
   • T. Cremer

   Original Investigations Pages: 1 - 6

2. Identification of functioning sweat pores and visualization of skin temperature patterns in X-linked hypohidrotic ectodermal dysplasia by whole body thermography

   • R. P. Clark
   • M. R. Goff
   • K. D. MacDermot

   Original Investigations Pages: 7 - 13

3. R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1)

   • Ei-ichi Takahashi
   • Tada-aki Hori
   • Ray White

   Original Investigations Pages: 14 - 16

4. Rare McArdle disease locus polymorphic site on 11q13 contains CpG sequence

   • Roger V. Lebo
   • Lee A. Anderson
   • Robert Fletterick

   Original Investigations Pages: 17 - 24

5. Selective advantage of fra (X) heterozygotes

   • F. Vogel
   • W. E. Crusio
   • M. Freund

   Original Investigations Pages: 25 - 32

6. Cytogenetic analysis of 400 sperm from three translocation heterozygotes

   • Renee H. Martin
   • Leona Barclay
   • S. Bea Fowlow

   Original Investigations Pages: 33 - 39

7. Ha-ras-1 alleles in Norwegian lung cancer patients

   • David Ryberg
   • Toril Tefre
   • Aage Haugen

   Original Investigations Pages: 40 - 44

8. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

   • Alan H. Beggs
   • Michel Koenig
   • Louis M. Kunkel

   Original Investigations Pages: 45 - 48

9. Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on a population from the Matera district

   • V. Calabrò
   • A. Giacobbe
   • G. Battistuzzi

   Original Investigations Pages: 49 - 53

10. Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome

    • D. Zhu
    • D. M. Alcorn
    • I. H. Maumenee

    Original Investigations Pages: 54 - 58

11. A new marker at DXS 115 useful for carrier detection in hemophilia A

    • Manfred Wehnert
    • Winnie Schröder
    • Falko H. Herrmann

    Original Investigations Pages: 59 - 60

12. Cloning of the breakpoints of a deletion associated with choroideremia

    • F. P. M. Cremers
    • F. Brunsmann
    • H. H. Ropers

    Original Investigations Pages: 61 - 64

13. The human VAV proto-oncogene maps to chromosome region 19p12→19p13.2

    • Cecile Martinerie
    • Linda A. Cannizzaro
    • Mariano Barbacid

    Original Investigations Pages: 65 - 68

14. Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy

    • Irma Dianzani
    • Marcella Devoto
    • Savio L. C. Woo

    Original Investigations Pages: 69 - 72

15. The human corticosteroid binding globulin gene is located on chromosome 14q31–q32.1 near two other serine protease inhibitor genes

    • Gilles-Eric Seralini
    • Dominique Bérubé
    • Geoffrey L. Hammond

    Original Investigations Pages: 73 - 75

16. Neither age nor sex influence the expression of folate sensitive common fragile sites on human chromosomes

    • Dominique F. C. M. Smeets
    • Gerard Merkx

    Original Investigations Pages: 76 - 78

17. The Na⁺/H⁺ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1

    • Christopher R. K. Dudley
    • Luis A. Giuffra
    • Stephen T. Reeders

    Original Investigations Pages: 79 - 83

18. Localization of the gene for human proliferating nuclear antigen/cyclin by in situ hybridization

    • Graham Webb
    • Peter Parsons
    • Georgia Chenevix-Trench

    Short Communications Pages: 84 - 86

19. An HhaI polymorphism is present in factor IX genes of Asian subjects

    • Alexander P. Reiner
    • Arthur R. Thompson

    Short Communications Pages: 87 - 88

20. Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy

    • James Skare
    • Hasan Yazici
    • Martha Skinner

    Short Communications Pages: 89 - 90

21. Detection by denaturing gradient gel electrophoresis of a new polymorphism in the apolipoprotein B gene

    • Maria Navajas
    • Anne-Marie Laurent
    • Gérard Roizès

    Short Communications Pages: 91 - 93

22. A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1

    • Nacer Abbas
    • Giuseppe Novelli
    • Bruno Dallapiccola

    Short Communications Pages: 94 - 98

23. Maternal transmission of ring chromosome 21

    • Ingo Kennerknecht
    • Gotthold Barbi
    • Walther Vogel

    Clinical Case Report Pages: 99 - 101

24. Crossover in a Spanish cystic fibrosis family

    • Esther Fernández
    • Manuela Villamar
    • Javier Benítez

    OriginalPaper Pages: 102 - 102