Table of contents

Research Article

• Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence. (1 April, 1985)

  E Tuckerman, T Webb, S E Bundey
• First trimester fetal diagnosis of genetic disorders: clinical evaluation of 250 cases. (1 April, 1985)

  B Brambati, G Simoni, C Danesino, A Oldrini, E Ferrazzi, L Romitti, G Terzoli, F Rossella, M Ferrari, M Fraccaro
• Cell surface abnormality in clones of skin fibroblasts from a carrier of Duchenne muscular dystrophy. (1 April, 1985)

  J Hillier, G E Jones, H E Statham, J A Witkowski, V Dubowitz
• A pedigree study of perinatally lethal renal disease. (1 April, 1985)

  A Bankier, M de Campo, R Newell, J G Rogers, D M Danks
• Necropsy findings in neonatal asphyxiating thoracic dystrophy. (1 April, 1985)

  S B Turkel, E J Diehl, J A Richmond
• An autosomal dominant syndrome with 'acromegaloid' features and thickened oral mucosa. (1 April, 1985)

  H E Hughes, P J McAlpine, D W Cox, S Philipps
• Kabuki make-up syndrome (Niikawa-Kuroki syndrome) associated with congenital heart disease. (1 April, 1985)

  S Ohdo, H Madokoro, T Sonoda, T Nishiguchi, K Kawaguchi, K Hayakawa
• The frequency of lactase phenotypes in Aymara children. (1 April, 1985)

  E Balanza, G Taboada
• The clinical features of the Cohen syndrome: further case reports. (1 April, 1985)

  C North, M A Patton, M Baraitser, R M Winter
• Dermatoglyphs in children with mitral valve prolapse. (1 April, 1985)

  J S Tay, W C Yip, H K Yap, B W Lee, H B Wong, S O Chay
• De novo paracentric inversion in an X chromosome. (1 April, 1985)

  H M Herr, S J Horton, C I Scott
• Monosomy 13q32.3----qter: report of two cases. (1 April, 1985)

  H Rivera, S A González-Flores, F Rivas, J Sánchez-Corona, M Moller, J M Cantú
• Congenital diaphragmatic hernia in half sibs. (1 April, 1985)

  A H Lipson, G Williams
• A case of suspected teratogenic holoprosencephaly. (1 April, 1985)

  M Stabile, A Bianco, S Iannuzzi, M C Buonocore, V Ventruto
• Tracheo-oesophageal anomalies in the Goldenhar anomalad. (1 April, 1985)

  A Mendelberg, I Ariel, P Mogle, I Arad
• Severe pseudoachondroplasia with parental consanguinity. (1 April, 1985)

  I D Young, J R Moore
• A case of malignant spinal cord ependymoma in association with a duplication of part of the long arm of chromosome 12. (1 April, 1985)

  B G Neville, A C Berry, Y Stoddart
• Interstitial deletion of chromosome 2. (1 April, 1985)

  S Marković, M Krstić, V Sulović, Z Radojković, S Adzić
• Familial occurrence of a pseudodicentric chromosome 21. (1 April, 1985)

  I Hancke, K Miller
• Extra euchromatic band in the qh region of chromosome 9. (1 April, 1985)

  Z Docherty, M A Hultén