Table of contents

Research Article

• Molecular euphoria. (1 April, 1986)

  R Harris
• Of mice and men, metals and mutations. (1 April, 1986)

  D M Danks
• Chromosome 1 in relation to human disease. (1 April, 1986)

  S Povey, J M Parrington
• The orofaciodigital (OFD) syndromes. (1 April, 1986)

  M Baraitser
• Familial partial lipodystrophy: two types of an X linked dominant syndrome, lethal in the hemizygous state. (1 April, 1986)

  J Köbberling, M G Dunnigan
• Partial lipoatrophy with insulin resistant diabetes and hyperlipidaemia (Dunnigan syndrome). (1 April, 1986)

  J Burn, M Baraitser
• Familial polyposis coli: growth characteristics of karyotypically variable cultured fibroblasts, response to epidermal growth factor and the tumour promoter 12-0-tetradecanoyl phorbol-13-acetate. (1 April, 1986)

  S H Rider, H A Mazzullo, M B Davis, J D Delhanty
• A new epsilon globin HincII variant fragment length in a South African Negroid family. (1 April, 1986)

  M Ramsay, J A Thomson, T Jenkins
• Abnormal haemoglobins among pregnant women from Mozambique. (1 April, 1986)

  M C Willcox, J Liljestrand, S Bergström
• Monosomy 8p: an easily overlooked syndrome. (1 April, 1986)

  A H Bröcker-Vriends, P D Mooij, F van Bel, G C Beverstock, J J van de Kamp
• The relationship between the acetylator and the sparteine hydroxylation polymorphisms. (1 April, 1986)

  D Harmer, D A Evans, L C Eze, M Jolly, E J Whibley
• Familial calcification of the basal ganglia with cerebrospinal fluid pleocytosis. (1 April, 1986)

  L Mehta, J Q Trounce, J R Moore, I D Young
• A Noonan-like short stature syndrome with sparse hair. (1 April, 1986)

  M Baraitser, M A Patton
• Duchenne muscular dystrophy in a female with a translocation involving Xp21. (1 April, 1986)

  N C Nevin, A E Hughes, M Calwell, J H Lim
• An additional case of Smith-Lemli-Opitz syndrome in a 46,XY infant with female external genitalia. (1 April, 1986)

  P R Scarbrough, K Huddleston, S C Finley
• Possible Waardenburg syndrome with gastrointestinal anomalies. (1 April, 1986)

  J Nutman, R Steinherz, Y Sivan, R M Goodman
• Multifocal meningiomas in a patient with a constitutional ring chromosome 22. (1 April, 1986)

  T Arinami, I Kondo, H Hamaguchi, S Nakajima
• Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement. (1 April, 1986)

  M H Bogart, C L Bradshaw, O W Jones, J E Schanberger
• Primary myelodysplastic syndrome with complex chromosomal rearrangements in a patient with Klinefelter's syndrome. (1 April, 1986)

  S M Abidi, M Griffiths, D G Oscier, G J Mufti, T J Hamblin
• Partial trisomy 6p and partial trisomy 22 resulting from 3:1 meiotic disjunction of maternal (6p;22q) translocation. (1 April, 1986)

  P R Scarbrough, A J Carroll, S C Finley, K Hamerick
• A study of retinitis pigmentosa in the city of Birmingham. (1 April, 1986)

  S Bundey, S J Crews
• Cornelia de Lange syndrome. (1 April, 1986)

  R M Winter
• A pedigree study of perinatally lethal renal disease. (1 April, 1986)

  A Hockey, J Crowhurst, I Walpole
• Mosaic trisomy 9. (1 April, 1986)

  J M Sánchez
• Spondyloepiphyseal dysplasia tarda with progressive arthropathy: a rare disorder frequently diagnosed among Arabs. (1 April, 1986)

  A S Teebi, S A Al Awadi