Y to X translocation in man H. van den BergheP. PetitJ. P. Fryns Original Investigations Pages: 129 - 141
Anomalous cellular proliferation in vitro associated with Huntington's disease David KirkJennifer M. ParringtonJean M. W. Bolt Original Investigations Pages: 143 - 154
Banding and spiralization of human metaphase chromosomes Ranjan Y. GoradiaBrian K. Davis Original Investigations Pages: 155 - 160
Red cell adenylate kinase phenotypes in the affective disorders Alan RundleBarbara SudellAlec Coppen Original Investigations Pages: 161 - 166
DIPI and DAPI: Fluorescence banding with only negligible fading W. SchnedlA. -V. MikelsaarO. Dann Original Investigations Pages: 167 - 172
Incidence of seizures and EEG abnormalities among offspring of epileptic patients Takayuki TsuboiShun'ichi Endo Original Investigations Pages: 173 - 189
Haplotype analysis of the linkage group HLA-A:HLA-B:Bf and its bearing on the interpretation of the linkage disequilibrium K. BenderA. MayerováT. Wienker Original Investigations Pages: 191 - 196
Pachytene mapping of the C 9 and acrocentric bivalents in the human oocyte J. M. LucianiMonique DevictorA. Stahl Original Investigations Pages: 197 - 204
Localisation régionale des gènes humains IDHS, MDHS, PGK, α-GAL, G6PD par l'hybridation cellulaire interspécifique Dominique WeilNguyen Van-CongJ. Frézal Original Investigations Pages: 205 - 211
UV-light induced sister chromatid exchanges in xeroderma pigmentosum lymphocytes A. Dorothee SchönwaldE. Passarge Original Investigations Pages: 213 - 218
β-Galactosidase deficiency in juvenile and adult patients Yoshiyuki SuzukiNorimasa NakamuraMasanori Uono Original Investigations Pages: 219 - 229
Erythrocyte superoxide dismutase in different racial groups in Malaysia Yao Sheng TengLuan Eng Lie-Injo Original Investigations Pages: 231 - 234
12pter → 12p 12.2: Possible assignment of human triose phosphate isomerase Marie-Odile RethoréJ. Cl. KaplanJ. Lejeune Short Communications Pages: 235 - 237
The 11q- syndrome: Another case report Marie T. MulcahyJoy Jenkyn Clinical Case Reports Pages: 239 - 242
Autosomal recessive microcephaly associated with chorioretinopathy J. M. CantúJ. A. RojasC. Manzano Clinical Case Reports Pages: 243 - 247