Book Reviews

	Issues and Reviews in Teratology Dian Donnai J Med Genet 1989; 26: 668. doi:10.1136/jmg.26.10.668 [PDF] [Request Permissions]
	The Foundations of Human Genetics Alan E H Emery J Med Genet 1989; 26: 668. doi:10.1136/jmg.26.10.668-a [PDF] [Request Permissions]
	Choices, Not Chances—An Essential Guide to your Heredity and Health A C Berry J Med Genet 1989; 26: 668-669. doi:10.1136/jmg.26.10.668-b [PDF] [Request Permissions]
	Medical Genetics: Principles and Practice Christine Garrett J Med Genet 1989; 26: 669. doi:10.1136/jmg.26.10.669 [PDF] [Request Permissions]
	Annual Review of Genetics Andrew P Read J Med Genet 1989; 26: 669-670. doi:10.1136/jmg.26.10.669-a [PDF] [Request Permissions]
	Nucleic Acid Probes in Diagnosis of Human Genetic Diseases P W Lunt J Med Genet 1989; 26: 670-671. doi:10.1136/jmg.26.10.670 [PDF] [Request Permissions]
	The Neural Crest Mary J Seller J Med Genet 1989; 26: 671. doi:10.1136/jmg.26.10.671 [PDF] [Request Permissions]

Research Article

	The calcitonin-CGRP gene in the infantile hypercalcaemia/Williams-Beuren syndrome. G A Hitman, L Garde, W Daoud, and G J Snodgrass J Med Genet 1989; 26: 609-613. doi:10.1136/jmg.26.10.609 [Abstract] [PDF] [Request Permissions]
	The molecular basis of beta thalassaemia in Bulgaria. L Kalaydjieva, A Eigel, and J Horst J Med Genet 1989; 26: 614-618. doi:10.1136/jmg.26.10.614 [Abstract] [PDF] [Request Permissions]
	A summary of 7q interstitial deletions and exclusion mapping of the gene for beta-glucuronidase. K Fagan, A Gill, R Henry, I Wilkinson, and B Carey J Med Genet 1989; 26: 619-625. doi:10.1136/jmg.26.10.619 [Abstract] [PDF] [Request Permissions]
	Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorder. H Rivera, O Zuffardi, P Maraschio, A Caiulo, C Anichini, R Scarinci, and R Vivarelli J Med Genet 1989; 26: 626-630. doi:10.1136/jmg.26.10.626 [Abstract] [PDF] [Request Permissions]
	Transient nephrotic syndrome after anaesthesia resulting from a familial cryofibrinogen precipitating at 35 degrees C. Y Lolin, P A Razis, P O'Gorman, M Hjelm, and A S Wierzbicki J Med Genet 1989; 26: 631-636. doi:10.1136/jmg.26.10.631 [Abstract] [PDF] [Request Permissions]
	Emery-Dreifuss syndrome. A E Emery J Med Genet 1989; 26: 637-641. doi:10.1136/jmg.26.10.637 [Abstract] [PDF] [Request Permissions]
	Familial mental retardation associated with balanced chromosome rearrangement rcp t(8;11)(q24.3;p15.1). H Sato, K Takaya, S Nihira, and H Fujita J Med Genet 1989; 26: 642-644. doi:10.1136/jmg.26.10.642 [Abstract] [PDF] [Request Permissions]
	A new interstitial deletion of 4q (q21.1::q22.1). K Fagan and A Gill J Med Genet 1989; 26: 644-647. doi:10.1136/jmg.26.10.644 [Abstract] [PDF] [Request Permissions]
	Cat eye syndrome associated with aganglionosis of the small and large intestine. J Ward, I A Sierra, and E D'Croz J Med Genet 1989; 26: 647-648. doi:10.1136/jmg.26.10.647 [Abstract] [PDF] [Request Permissions]
	A single maxillary incisor as a manifestation of an ectodermal dysplasia. I Buntinx and M Baraitser J Med Genet 1989; 26: 648-651. doi:10.1136/jmg.26.10.648 [Abstract] [PDF] [Request Permissions]
	Interstitial deletion, del(4)(q33q35.1), in a mother and two children. M A Curtis, R A Smith, J Sibert, and H E Hughes J Med Genet 1989; 26: 652-654. doi:10.1136/jmg.26.10.652 [Abstract] [PDF] [Request Permissions]
	Maternal translocation (9;18) with two abnormal offspring each with different chromosome derivatives. M Pearson, C Riske, and J E Allanson J Med Genet 1989; 26: 655-658. doi:10.1136/jmg.26.10.655 [Abstract] [PDF] [Request Permissions]
	Central nervous system malformations in Mohr's syndrome. W Reardon, M G Harbord, M A Hall-Craggs, B Kendall, E M Brett, and M Baraitser J Med Genet 1989; 26: 659-663. doi:10.1136/jmg.26.10.659 [Abstract] [PDF] [Request Permissions]
	Unknown syndrome: congenital heart disease, ptosis, hypodontia, and craniosynostosis. L Mehta, I Lewis, and M A Patton J Med Genet 1989; 26: 664-665. doi:10.1136/jmg.26.10.664 [Abstract] [PDF] [Request Permissions]
	Unknown syndrome in sibs: microcephaly, seizures, mental retardation, congenital heart disease, and skeletal abnormalities. G E Holmes and R N Schimke J Med Genet 1989; 26: 665-666. doi:10.1136/jmg.26.10.665 [Abstract] [PDF] [Request Permissions]
	Updated results of the thalassaemia prevention programme carried out in Latium. I Bianco, B Graziani, M Lerone, D Ponzini, M C Aliquo, and E Foglietta J Med Genet 1989; 26: 667. doi:10.1136/jmg.26.10.667 [PDF] [Request Permissions]