1. Y to X translocation in man

   • H. van den Berghe
   • P. Petit
   • J. P. Fryns

   Original Investigations Pages: 129 - 141

2. Anomalous cellular proliferation in vitro associated with Huntington's disease

   • David Kirk
   • Jennifer M. Parrington
   • Jean M. W. Bolt

   Original Investigations Pages: 143 - 154

3. Banding and spiralization of human metaphase chromosomes

   • Ranjan Y. Goradia
   • Brian K. Davis

   Original Investigations Pages: 155 - 160

4. Red cell adenylate kinase phenotypes in the affective disorders

   • Alan Rundle
   • Barbara Sudell
   • Alec Coppen

   Original Investigations Pages: 161 - 166

5. DIPI and DAPI: Fluorescence banding with only negligible fading

   • W. Schnedl
   • A. -V. Mikelsaar
   • O. Dann

   Original Investigations Pages: 167 - 172

6. Incidence of seizures and EEG abnormalities among offspring of epileptic patients

   • Takayuki Tsuboi
   • Shun'ichi Endo

   Original Investigations Pages: 173 - 189

7. Haplotype analysis of the linkage group HLA-A:HLA-B:Bf and its bearing on the interpretation of the linkage disequilibrium

   • K. Bender
   • A. Mayerová
   • T. Wienker

   Original Investigations Pages: 191 - 196

8. Pachytene mapping of the C 9 and acrocentric bivalents in the human oocyte

   • J. M. Luciani
   • Monique Devictor
   • A. Stahl

   Original Investigations Pages: 197 - 204

9. Localisation régionale des gènes humains IDH_S, MDH_S, PGK, α-GAL, G6PD par l'hybridation cellulaire interspécifique

   • Dominique Weil
   • Nguyen Van-Cong
   • J. Frézal

   Original Investigations Pages: 205 - 211

10. UV-light induced sister chromatid exchanges in xeroderma pigmentosum lymphocytes

    • A. Dorothee Schönwald
    • E. Passarge

    Original Investigations Pages: 213 - 218

11. β-Galactosidase deficiency in juvenile and adult patients

    • Yoshiyuki Suzuki
    • Norimasa Nakamura
    • Masanori Uono

    Original Investigations Pages: 219 - 229

12. Erythrocyte superoxide dismutase in different racial groups in Malaysia

    • Yao Sheng Teng
    • Luan Eng Lie-Injo

    Original Investigations Pages: 231 - 234

13. 12pter → 12p 12.2: Possible assignment of human triose phosphate isomerase

    • Marie-Odile Rethoré
    • J. Cl. Kaplan
    • J. Lejeune

    Short Communications Pages: 235 - 237

14. The 11q- syndrome: Another case report

    • Marie T. Mulcahy
    • Joy Jenkyn

    Clinical Case Reports Pages: 239 - 242

15. Autosomal recessive microcephaly associated with chorioretinopathy

    • J. M. Cantú
    • J. A. Rojas
    • C. Manzano

    Clinical Case Reports Pages: 243 - 247