Table of contents
December 1995 - Volume 32 - 12
Research Article
- Psychological aspects of von Recklinghausen neurofibromatosis (NF1) (1 December, 1995)
- X inactivation of the FMR1 fragile X mental retardation gene. (1 December, 1995)
- Ophthalmic genetics: a genealogical guide to sources in England and Wales. (1 December, 1995)
- No evidence of genetic heterogeneity in dominant optic atrophy. (1 December, 1995)
- Further delineation of the partial proximal trisomy 10q syndrome. (1 December, 1995)
- The Irish cystic fibrosis database. (1 December, 1995)
- A large multisite cancer family is linked to BRCA2. (1 December, 1995)
- Familial café au lait spots: a variant of neurofibromatosis type 1. (1 December, 1995)
- Partial disomy of Xp and the presence of SRY in a phenotypic female. (1 December, 1995)
- Del(3) (p25.3) without phenotypic effect. (1 December, 1995)
- Leukaemia and Sellafield: is there a heritable link? (1 December, 1995)
Abstracts
- Medical genetics: advances in brief (1 December, 1995)
- Medical genetics: advances in brief (1 December, 1995)
- Medical genetics: advances in brief (1 December, 1995)
- Medical genetics: advances in brief (1 December, 1995)
Letters to the Editor
- Reply (1 December, 1995)
Book Reviews
- Prenatal Diagnosis: The Human Side (1 December, 1995)
- Friendly Fire: Explaining Autoimmune Disease (1 December, 1995)
- Secrets in the Genes (1 December, 1995)
- The Molecular Genetics of Cancer (1 December, 1995)
- Familial Adenomatous Polyposis and Other Polyposis Syndromes (1 December, 1995)
- Animals with Novel Genes (1 December, 1995)