Table of contents

Research Article

• A reappraisal of the CHARGE association. (1 March, 1988)

  C A Oley, M Baraitser, D B Grant
• Further delineation of the G syndrome: a manageable genetic cause of infantile dysphagia. (1 March, 1988)

  G N Wilson, W J Oliver
• Intellectual development in Apert's syndrome: a long term follow up of 29 patients. (1 March, 1988)

  M A Patton, J Goodship, R Hayward, R Lansdown
• Familial spastic paraplegia, bilateral sensorineural deafness, and intellectual retardation associated with a progressive nephropathy. (1 March, 1988)

  J S Fitzsimmons, A R Watson, D Mellor, P R Guilbert
• Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome. (1 March, 1988)

  P Maraschio, O Zuffardi, T Dalla Fior, L Tiepolo
• Family size limitation: a method for demonstrating recessive inheritance. (1 March, 1988)

  J F Brookfield, R J Pollitt, I D Young
• The frequency of consanguineous marriage among British Pakistanis. (1 March, 1988)

  A Darr, B Modell
• Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8). (1 March, 1988)

  O W Quarrell, S Youngman, M Sarfarazi, P S Harper
• Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemia. (1 March, 1988)

  A Metaxotou-Mavromati, C Kattamis, L Matathia, M Tzetis, E Kanavakis
• Sclerosteosis. (1 March, 1988)

  P Beighton
• Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome. (1 March, 1988)

  H Santos, J Mateus, M J Leal
• Unusual dual genital duct remnants in true hermaphroditism. (1 March, 1988)

  C Williams, I A Hughes
• De novo 10q23 interstitial deletion. (1 March, 1988)

  M A Mori, F Gomez-Sabrido, A Diaz de Bustamante, I Pinel, M L Martinez-Frias
• Interstitial deletion (6) (q11----q15) in an infant with congenital abnormalities. (1 March, 1988)

  H R Slater, A Robb, L A Forsyth, D A Hamilton, M C Clark, C A Galloway
• Terminal deletion of chromosome 1(q43) in a female infant. (1 March, 1988)

  G P Garani, L Tamisari, S Volpato, V Vigi
• Anomalous X chromosome inactivation: the link between female zygotes, monozygotic twinning, and neural tube defects? (1 March, 1988)