Table of contents

Research Article

• The fragile X syndrome: the patients and their chromosomes. (1 April, 1984)

  M A De Arce, A Kearns
• Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus. (1 April, 1984)

  P Ward, S Packman, W Loughman, M Sparkes, R Sparkes, A McMahon, T Gregory, A Ablin
• Breast cancer, genetics, and age at first pregnancy. (1 April, 1984)

  H T Lynch, W A Albano, M A Layton, W J Kimberling, J F Lynch
• On the identification and frequency of the J and K cholinesterase phenotypes in a Caucasian population. (1 April, 1984)

  R T Evans, J Wardell
• Late infantile autosomal recessive myotonia, mental retardation, and skeletal abnormalities: a new autosomal recessive syndrome. (1 April, 1984)

  A Richieri-Costa, S M Garcia da Silva, O Frota-Pessoa
• Multiple endocrine neoplasia type 2 (Sipple's syndrome): clinical and cytogenetic analysis of a kindred. (1 April, 1984)

  A Zatterale, M Stabile, V Nunziata, G Di Giovanni, R Vecchione, V Ventruto
• Familial multiple naevi flammei. (1 April, 1984)

  A Shuper, P Merlob, B Garty, I Varsano
• Familial occurrence of unilateral giant breasts in Nigeria: a possible new genetic entity. (1 April, 1984)

  O A Badejo
• Delta beta-thalassaemia in southern Italy: evidence for a single mutational event. (1 April, 1984)

  A Carè, N M Sposi, A Giampaolo, T Improta, M Calandrini, M Petrini, M Marinucci, A Tagarelli, C Brancati
• A computerised data base for the diagnosis of rare dysmorphic syndromes. (1 April, 1984)

  R M Winter, M Baraitser, J M Douglas
• The 3-M syndrome. (1 April, 1984)

  R M Winter, M Baraitser, D B Grant, M A Preece, C M Hall
• Gossypol induces DNA strand breaks in human fibroblasts and sister chromatid exchanges in human lymphocytes in vitro. (1 April, 1984)

  M Nordenskjöld, B Lambert
• Trisomy 1q24----1q41 in two sibs with an insertion in an inverted chromosome 4. (1 April, 1984)

  C Stoll, M P Roth, B Dott
• Treated glass coverslips for in situ culture of amniotic cells: better cell adhesion and growth than on plastic. (1 April, 1984)

  V Pecile, N Archidiacono, M Rocchi
• Trisomy 5p: a second case occurring in a previously described kindred. (1 April, 1984)

  M Vowles, A McDermott, I Janota
• A case of deletion 2q35----qter and a peculiar phenotype. (1 April, 1984)

  J M Sánchez, A M Pantano
• Familial pericentric inversion (13) detected by antenatal diagnosis. (1 April, 1984)

  E L Maltby
• Trisomy 18 phenotype in a patient with an isopseudodicentric 18 chromosome. (1 April, 1984)

  E A Wulfsberg, R S Sparkes, I J Klisak, A Teng
• A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia. (1 April, 1984)

  R Galanello, L Maccioni, M C Rosatelli, P Ibba, A M Nurchi, A Cao
• Interpretation of RFLP linkage data. (1 April, 1984)

  J F Clayton
• Haemoglobin O Arab (B121 Glu-Lys) in Turkish Cypriot population. (1 April, 1984)

  S Cin, N Akar, A Arcasoy, A O Cavdar, S Dedeoğlu
• Incidence of pyloric stenosis in British Columbia over a 12 year period. (1 April, 1984)

  A D Sadovnick, P A Baird