Trisomy 9q—. A variant of the 9p trisomy syndrome Willard R. CenterwallCarol A. MayeskiChul C. Cha Original Investigations Pages: 91 - 98
Familial true hermaphrodism in three siblings S. ArmendaresF. SalamancaA. Parra Original Investigations Pages: 99 - 109
Lipodystrophy of the extremities. A dominantly inherited syndrome associated with lipatrophic diabetes J. KöbberlingB. WillmsW. Creutzfeldt Original Investigations Pages: 111 - 120
Haemoglobin synthesis in 28 obligatory cases for α-thalassemia traits Sa-nga PootrakulSuwat SapprapaRomsai Suwanik Original Investigations Pages: 121 - 126
Cytogenetic effects of cyclophosphamide on mouse spermatogonia R. Rathenberg Original Investigations Pages: 135 - 140
Cystinuric heterozygotes and cystine-loading R. MinamiK. OlekP. Wardenbach Short Communications Pages: 145 - 149
Statistical evaluation of a new method to detect carriers of phenylketonuria R. MinamiK. OlekP. Wardenbach Short Communications Pages: 151 - 154
Familial correlations in the judgment of numerousness Ruth Guttman Short Communications Pages: 161 - 164
Stability of X chromosomal inactivation in human somatic cells transformed by SV-40 Giovanni RomeoBarbara R. Migeon Short Communications Pages: 165 - 170
Extra-hepatic storage of copper K. HeydornElse DamsgaardJ. Weber Clinical Case Reports Pages: 171 - 175