Table of contents

Research Article

• Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma. (1 April, 1988)

  V Greger, S Kerst, E Messmer, W Höpping, E Passarge, B Horsthemke
• Linkage analysis of X linked retinitis pigmentosa in the Irish population. (1 April, 1988)

  G J Farrar, M T Geraghty, J M Moloney, D J McConnell, P Humphries
• A family showing apparent X linked inheritance of both anencephaly and spina bifida. (1 April, 1988)

  O Jensson, A Arnason, H Gunnarsdottir, I Petursdottir, R Fossdal, S Hreidarsson
• Autosomal recessive inheritance of Nager acrofacial dysostosis. (1 April, 1988)

  J Chemke, B M Mogilner, I Ben-Itzhak, L Zurkowski, D Ophir
• Familial polyposis coli: no evidence for increased sensitivity to mitomycin C. (1 April, 1988)

  H A Mazzullo, J Attwood, J D Delhanty
• Expression of fra(10)(q25) in peripheral blood and bone marrow in familial neutropenia. (1 April, 1988)

  J A Holmes, P W Thompson
• Theoretical recurrence risks for cleft lip derived from a population of consecutive newborns. (1 April, 1988)

  R Tenconi, M Clementi, L Turolla
• Hypothyroidism and sex chromosomes. (1 April, 1988)

  C Sarri, G B Côté, C Mengreli, I Lambadaridis, S Pantelakis
• Klippel-Trenaunay-Weber syndrome (angio-osteohypertrophy syndrome). (1 April, 1988)

  D L Viljoen
• Medical genetics in China. (1 April, 1988)

  L Hui-Yuan
• Duplication 17q mosaicism: an infant with features of Ellis-van Creveld syndrome. (1 April, 1988)

  A Serotkin, J Stamberg, L Waber
• De novo partial trisomy 15q (proximal type). (1 April, 1988)

  T J Herweijer, J W Oorthuys, N J Leschot
• Clinical consequences of deletion 1p35. (1 April, 1988)

  S L Wenger, M W Steele, D J Becker
• A duplication/deficient X chromosome in a girl with mental retardation and dysmorphic features. (1 April, 1988)

  I C Barnes, D Curtis, S L Duncan
• Martsolf's syndrome in a non-Jewish boy. (1 April, 1988)

  P Strisciuglio, M Costabile, M Esposito, S Di Maio
• Unknown syndrome: mental retardation with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes' disease of the hip. (1 April, 1988)

  C Garrett, J H Tripp
• Unknown syndrome: microcephaly, facial clefting, and preaxial polydactyly. (1 April, 1988)

  F M Howard, I D Young
• Abstracts of the meeting of the Clinical Genetics Society. 20 and 21 November 1987, London. (Joint meeting with the Skeletal Dysplasia Group) (1 April, 1988)