Table of contents
September 1991 - Volume 28 - 9
Research Article
- Chromosome in situ suppression hybridisation in clinical cytogenetics. (1 September, 1991)
- Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17. (1 September, 1991)
- Do familial neural tube defects breed true? (1 September, 1991)
- 49,XXXXY syndrome: behavioural and developmental profiles. (1 September, 1991)
- Birth distribution in cystic fibrosis in Saguenay-Lac-St-Jean, Quebec, Canada. (1 September, 1991)
- Microcephaly-cardiomyopathy: a new autosomal recessive phenotype? (1 September, 1991)
- Postaxial acrofacial dysostosis (Miller) syndrome: a new case. (1 September, 1991)
- Mosaic partial trisomy 17q2. (1 September, 1991)
- The frequency of mental retardation in hypochondroplasia. (1 September, 1991)
- Unusual inheritance of Becker type muscular dystrophy. (1 September, 1991)
- Haematometra in the Langer-Giedion syndrome. (1 September, 1991)
Book Reviews
- Genomic Imprinting (1 September, 1991)
- Chromosome Banding (1 September, 1991)