Table of contents

Research Article

• Chromosomal breakage in normal and fragile X subjects using low folate culture conditions. (1 December, 1983)

  M Vekemans, B Popovich, D Rosenblatt, P Monroe
• Huntington's disease in monozygotic twins reared apart. (1 December, 1983)

  L Sudarsky, R H Myers, T M Walshe
• Huntington's disease and leprosy in a New Guinea Highlander. (1 December, 1983)

  E M Scrimgeour
• Agenesis of the corpus callosum in two brothers. (1 December, 1983)

  W G Wilson, J M Kennaugh, J P Kugler, J F Reynolds
• Study of a form of pulverulent cataract in a large kindred. (1 December, 1983)

  M Stabile, A Amoriello, S Capobianco, M L Cavaliere, N Conte, C De Rosa, S Ruoppo, V Sorrentino, V Ventruto
• Severe cardiac anomalies in sibs with Larsen syndrome. (1 December, 1983)

  P Strisciuglio, G Sebastio, G Andria, S Maione, V Raia
• Phenotype-genotype correlation in haemoglobin H disease in childhood. (1 December, 1983)

  R Galanello, M Pirastu, M A Melis, E Paglietti, P Moi, A Cao
• The haemoglobin pattern of sickle cell and haemoglobin C beta +-thalassaemia in Liberia. (1 December, 1983)

  M Willcox
• Syndrome of polydactyly, cleft lip, lingual hamartomas, renal hypoplasia, hearing loss, and psychomotor retardation: variant of the Mohr syndrome or a new syndrome? (1 December, 1983)

  J F Mattei, S Aymé
• Osteoglophonic dwarfism in two generations. (1 December, 1983)

  R I Kelley, P F Borns, D Nichols, E H Zackai
• Hereditary costovertebral dysplasia with malignant cerebral tumour. (1 December, 1983)

  T J David, A Glass
• Malformations associated with congenital absence of the gall bladder. (1 December, 1983)

  S B Turkel, V Swanson, P Chandrasoma
• Spatial relationship of human X and Y chromosomes at somatic metaphase. (1 December, 1983)

  D Dosik, R S Verma
• A simple technique for obtaining prometaphase chromosomes from lymphocytes. (1 December, 1983)

  J V Shah, R S Verma, J Rodriguez, H Dosik
• Huntington's chorea arising as a fresh mutation. (1 December, 1983)

  M Baraitser, J Burn, T A Fazzone
• Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD. (1 December, 1983)

  B S Emanuel, E H Zackai, S H Tucker
• Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33). (1 December, 1983)

  S A Al-Awadi, T I Farag, K Naguib, A Teebi, A Cuschieri, S Al-Othman, T S Sundareshan
• Partial trisomy 14q24 leads to qter. (1 December, 1983)

  D R Romain, L M Columbano-Green, R H Smythe, R G Parfitt, O Gebbie, C J Chapman, M Wall
• X chromosome replication patterns in a case of X;9 balanced translocation. (1 December, 1983)

  G Filippi, V Pecile, N Archidiacono, E Baragino, G Auber, M Rocchi
• Reciprocal translocation 14q;21q in a patient with the Brachmann-de Lange syndrome. (1 December, 1983)

  W G Wilson, J M Kennaugh, J P Kugler, H E Wyandt
• De novo duplication of the 7q11 leads to q22 region. (1 December, 1983)

  N B Kardon, L Pollack, J Davis, A Broekman, M Krauss
• De novo interstitial direct duplication of 15q: 46,XY,dir dup(15) (pter leads to q24::q14 leads to q21 X 1::q24 leads to qter). (1 December, 1983)

  H M Herr, C I Scott, S J Horton
• A father and daughter with fragile X chromosome. (1 December, 1983)

  S Morić-Petrović, Z Laća
• Metatarsus adductus in two brothers with Aarskog syndrome. (1 December, 1983)

  D L Hurst
• Familial hypogonadism with a balanced reciprocal 1;12 translocation. (1 December, 1983)

  D Handelsman, A Smith