Cytogerontology since 1881: A reappraisal of August Weismann and a review of modern progress Thomas B. L. KirkwoodThomas Cremer Review Articles Pages: 101 - 121
The genetic linkage between the PKU locus and the loci for Amylase1, Amylase2, Fy, PGM1, and Rh and the question of assignment of the PKU locus to chromosome No. 1 A. KnappR. TintschewaK. E. Biebler Original Investigations Pages: 122 - 125
Different patterns of X chromosome inactivity in lymphocytes and fibroblasts of a human balanced X; autosome translocation Bernard HellkuhlAlbert de la ChapelleKarl-Heinz Grzeschik Original Investigations Pages: 126 - 129
Distamycin A-DAPI banding of nonfluorescent Y (Ynf) chromosomes in 45,X/46,XYnf mosaicism Lawrence P. WisniewskiKurt Hirschhorn Original Investigations Pages: 130 - 132
Nonfluorescent Y chromosomes. Cytologic evidence of origin Ellen MagenisTimothy Donlon Original Investigations Pages: 133 - 138
An attempt to define 1qh+, 9qh+, and 16qh+ Ursula FriedrichAage Juhl Therkelsen Original Investigations Pages: 139 - 144
Genetic variants of placental alkaline phosphatase as detected by a monoclonal antibody José Luis MillánGunhild BeckmanTorgny Stigbrand Original Investigations Pages: 145 - 149
Tangier disease: Heterozygote detection and linkage analysis Brian K. SuarezGustav SchonfeldRobert S. Sparkes Original Investigations Pages: 150 - 156
Exclusion of linkage between the loci for multiple endocrine neoplasia type-2 (MEN-2) and HLA Nancy E. SimpsonJudy Falk Original Investigations Pages: 157 - 157
Human β-galactosidase and α-neuraminidase deficient mucolipidosis: Genetic complementation analysis of the neuraminidase deficiency O. Thomas MuellerThomas B. Shows Original Investigations Pages: 158 - 162
X-linked genes of the H-Y antigen system in the wood lemming (Myopus schisticolor) Ulf WibergAntonia MayerováUlrich Wolf Original Investigations Pages: 163 - 166
Diagnosis of Hunter's syndrome carriers; Radioactive sulphate incorporation into fibroblasts in the presence of fructose 1-phosphate Tønne TønnesenClaus LykkelundFlemming Güttler Original Investigations Pages: 167 - 171
Of rabbit and man: Comparative gene mapping Joëlle SoulieJ. de Grouchy Original Investigations Pages: 172 - 175
Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis: 2. Genetic polymorphism of lymphocyte cytosol 64K polypeptide Hideo HamaguchiMichiko YamadaIkuko Kondo Original Investigations Pages: 176 - 180
De novo mutations producing unstable Hbs or Hbs M. G. StamatoyannopoulosP. E. Nute Original Investigations Pages: 181 - 188
Glucose-6-phosphate dehydrogenase deficiency in Papua New Guinea K. ChockkalingamP. G. BoardG. T. Nurse Original Investigations Pages: 189 - 192
Retinoblastoma in a boy with a de novo mutation of a 13/18 translocation: The assumption that the retinoblastoma locus is at 13q141, particularly at the distal portion of it T. MotegiM. KomatsuK. Minoda Clinical Case Reports Pages: 193 - 195
Ovarian development in 46,XY gonadal dysgenesis Marcia H. RussellStephen S. WachtelIan M. Burr Clinical Case Reports Pages: 196 - 199
Centric fission of chromosome No. 7 in three generations Dietmar Janke Clinical Case Reports Pages: 200 - 201
Cytogenetic studies of a family with trisomy 21 mosaicism in two successive generations as the cause of Down's syndrome W. WernerF. H. HerrmannB. John Clinical Case Reports Pages: 202 - 204
The crucial band for phenotype of trisomy 18 J. MückeU. TrautmannH. Theile Letter to the Editors Pages: 205 - 205
Cryptorchidism and hypogenitalism in X-linked recessive ichthyosis vulgaris H. TraupeH. H. Ropers Letter to the Editors Pages: 206 - 206
