Editorials

	Medical genetics around the world Peter S Harper J Med Genet 1988; 25: 1. doi:10.1136/jmg.25.1.1 [PDF] [Request Permissions]

Book Reviews

	Teratogen Update: Environmentally Induced Birth Defect Risks Dian Donnai J Med Genet 1988; 25: 66. doi:10.1136/jmg.25.1.66 [PDF] [Request Permissions]
	Perinatal Genetics: Diagnosis and Treatment Jonathan Zonana J Med Genet 1988; 25: 66-67. doi:10.1136/jmg.25.1.66-a [PDF] [Request Permissions]
	Annual Review of Genetics Thaddeus E Kelly J Med Genet 1988; 25: 67. doi:10.1136/jmg.25.1.67 [PDF] [Request Permissions]
	The Chromosomes and Their Disorders. An Introduction for Clinicians D C Siggers J Med Genet 1988; 25: 67. doi:10.1136/jmg.25.1.67-a [PDF] [Request Permissions]
	A Clinician's View of Neuromuscular Diseases J R Sibert J Med Genet 1988; 25: 68. doi:10.1136/jmg.25.1.68 [PDF] [Request Permissions]
	The Man Behind the Syndrome Alan E H Emery J Med Genet 1988; 25: 68. doi:10.1136/jmg.25.1.68-a [PDF] [Request Permissions]
	Malformations in Children from One to Seven Years. A Report from the Collaborative Perinatal Project Dian Donnai J Med Genet 1988; 25: 68-69. doi:10.1136/jmg.25.1.68-b [PDF] [Request Permissions]
	The Hemoglobinopathies W G Wood J Med Genet 1988; 25: 69. doi:10.1136/jmg.25.1.69 [PDF] [Request Permissions]
	Evolution from Molecules to Men Alan E H Emery J Med Genet 1988; 25: 69-70. doi:10.1136/jmg.25.1.69-a [PDF] [Request Permissions]
	The Developmental Field Concept H E Hughes J Med Genet 1988; 25: 70. doi:10.1136/jmg.25.1.70 [PDF] [Request Permissions]
	Practical Genetics Mansoor Sarfarazi J Med Genet 1988; 25: 70. doi:10.1136/jmg.25.1.70-a [PDF] [Request Permissions]
	Gametogenesis and the Early Embryo Ian J Jackson J Med Genet 1988; 25: 71. doi:10.1136/jmg.25.1.71 [PDF] [Request Permissions]

Research Article

	Medical genetics in Hungary. A Czeizel J Med Genet 1988; 25: 2-8. doi:10.1136/jmg.25.1.2 [PDF] [Request Permissions]
	Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome. K E Davies, T J Smith, S Bundey, A P Read, T Flint, M Bell, and A Speer J Med Genet 1988; 25: 9-13. doi:10.1136/jmg.25.1.9 [Abstract] [PDF] [Request Permissions]
	Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophy. J Goodship, S Malcolm, M E Robertson, and M E Pembrey J Med Genet 1988; 25: 14-19. doi:10.1136/jmg.25.1.14 [Abstract] [PDF] [Request Permissions]
	Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindreds. S H Sacks, J M Old, S T Reeders, D J Weatherall, A S Douglas, J H Winter, and C R Rizza J Med Genet 1988; 25: 20-24. doi:10.1136/jmg.25.1.20 [Abstract] [PDF] [Request Permissions]
	The use of restriction fragment length polymorphisms in prenatal diagnosis of dihydropteridine reductase deficiency. H H Dahl, S Wake, R G Cotton, and D M Danks J Med Genet 1988; 25: 25-28. doi:10.1136/jmg.25.1.25 [Abstract] [PDF] [Request Permissions]
	Polymorphic acetylation of sulphamethazine in a Zimbabwe population. C F Nhachi J Med Genet 1988; 25: 29-31. doi:10.1136/jmg.25.1.29 [Abstract] [PDF] [Request Permissions]
	Osteoporosis-pseudoglioma syndrome with congenital heart disease: a new association. A S Teebi, S A Al-Awadi, M J Marafie, R A Bushnaq, and S Satyanath J Med Genet 1988; 25: 32-36. doi:10.1136/jmg.25.1.32 [Abstract] [PDF] [Request Permissions]
	Association of syndactyly, ectodermal dysplasia, and cleft lip and palate: report of two sibs from Turkey. G Ogur and M Yüksel J Med Genet 1988; 25: 37-40. doi:10.1136/jmg.25.1.37 [Abstract] [PDF] [Request Permissions]
	Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome. M Baraitser and R M Winter J Med Genet 1988; 25: 41-43. doi:10.1136/jmg.25.1.41 [Abstract] [PDF] [Request Permissions]
	Association of an ataxia indistinguishable from Friedreich's ataxia and congenital glaucoma in a family: a new syndrome. O Combarros, J Calleja, C Leno, and J Berciano J Med Genet 1988; 25: 44-46. doi:10.1136/jmg.25.1.44 [Abstract] [PDF] [Request Permissions]
	Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES syndrome) C Oley and M Baraitser J Med Genet 1988; 25: 47-51. doi:10.1136/jmg.25.1.47 [PDF] [Request Permissions]
	Prenatal diagnosis of inv(X)(q12q28) in a male fetus. R L Neu, H S Brar, and B J Koos J Med Genet 1988; 25: 52-53. doi:10.1136/jmg.25.1.52 [Abstract] [PDF] [Request Permissions]
	A recognisable short stature syndrome with premature aging and pigmented naevi. M Baraitser, J Insley, and R M Winter J Med Genet 1988; 25: 53-56. doi:10.1136/jmg.25.1.53 [Abstract] [PDF] [Request Permissions]
	VATER association: report of a case with three unreported malformations. M Dusmet, F Fête, A Crusi, and J N Cox J Med Genet 1988; 25: 57-60. doi:10.1136/jmg.25.1.57 [Abstract] [PDF] [Request Permissions]
	Two whole arm reciprocal translocations. A Smith, R Murray, and G den Dulk J Med Genet 1988; 25: 61. doi:10.1136/jmg.25.1.61 [PDF] [Request Permissions]
	Royal Society discussion meeting: Prevention and Avoidance of Genetic Disease, held on 29 to 30 April 1987 at the Royal Society. N Haites and A W Johnston J Med Genet 1988; 25: 62-63. doi:10.1136/jmg.25.1.62 [PDF] [Request Permissions]
	Expression of fragile X chromosome and possible deletion in successive cell divisions. Z Laca and S Brankovic J Med Genet 1988; 25: 64. doi:10.1136/jmg.25.1.64 [PDF] [Request Permissions]
	Noonan syndrome. A E Lin J Med Genet 1988; 25: 64-65. doi:10.1136/jmg.25.1.64-a [PDF] [Request Permissions]
	The population genetics of Duchenne muscular dystrophy. J H Edwards J Med Genet 1988; 25: 65. doi:10.1136/jmg.25.1.65 [PDF] [Request Permissions]