Table of contents

Research Article

• Gene mapping and chromosome 19. (1 February, 1986)

  D J Shaw, J D Brook, A L Meredith, H G Harley, M Sarfarazi, P S Harper
• Dubowitz syndrome. (1 February, 1986)

  R M Winter
• Meiotic recombination between two polymorphic restriction sites within the beta globin gene cluster. (1 February, 1986)

  J M Old, C Heath, A Fitches, S L Thein, A J Jeffreys, M Petrou, B Modell, D J Weatherall
• Evidence against the structural gene encoding type II collagen (COL2A1) as the mutant locus in achondroplasia. (1 February, 1986)

  D Ogilvie, P Wordsworth, E Thompson, B Sykes
• X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia. (1 February, 1986)

  J Halliday, C W Chow, D Wallace, D M Danks
• Autosomal recessive or sex linked recessive: a counselling dilemma. (1 February, 1986)

  I D Young, Z Nugent, T Grimm
• A computer programme to calculate risk in X linked disorders using multiple marker loci. (1 February, 1986)

  J F Clayton
• A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional information. (1 February, 1986)

  M Sarfarazi, H Williams
• Prenatal diagnosis of bullous ichthyosiform erythroderma: detection of tonofilament clumps in fetal epidermal and amniotic fluid cells. (1 February, 1986)

  R A Eady, D B Gunner, L D Carbone, F D Bricarelli, C M Gosden, C H Rodeck
• Early prenatal investigation of a pregnancy at risk of adenosine deaminase deficiency using chorionic villi. (1 February, 1986)

  D A Aitken, D H Gilmore, C A Frew, M E Ferguson-Smith, M J Carty, W R Chatfield
• Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy. (1 February, 1986)

  S M Huson, A L Meredith, M Sarfarazi, D J Shaw, D A Compston, P S Harper
• Genetic analysis of malformations causing perinatal mortality. (1 February, 1986)

  I D Young, A B Rickett, M Clarke
• The lethal multiple congenital anomaly syndrome of polydactyly, sex reversal, renal hypoplasia, and unilobular lungs. (1 February, 1986)

  D Donnai, I D Young, W G Owen, S A Clark, P F Miller, W F Knox
• Sensitivity to ultraviolet radiation in a dominantly inherited form of xeroderma pigmentosum. (1 February, 1986)

  F P Imray, A Hockey, W Relf, R G Ramsay, C Kidson
• A case of Fryns syndrome. (1 February, 1986)

  I D Young, K Simpson, R M Winter
• Umbilical cord hernia in a child with autosomal recessive chondrodysplasia punctata. (1 February, 1986)

  O Chandavasu, F Desposito
• Trisomy 14 mosaicism in a 2 year old girl. (1 February, 1986)

  M B Petersen, L O Vejerslev, B Beck
• First trimester diagnosis from chorionic villi of a der(15),t(9;15)(q33;q14)mat identified by DA/DAPI staining. (1 February, 1986)

  J O Van Hemel, D F Majoor-Krakauer, M G Jahoda, E S Sachs
• A three way translocation in mother and daughter. (1 February, 1986)

  R J Gardner, N A Monk, G J Allen, M I Parslow
• Familial inv(1)(p36.3q12) associated with sterility. (1 February, 1986)

  A Barros, M C Tavares, M P Gomes, M P Tavares
• Complex translocation involving chromosomes Y, 1, and 3 resulting in deletion of segment 3q23----q25. (1 February, 1986)

  S A Al-Awadi, K K Naguib, T I Farag, A S Teebi, A Cuschieri, S A Al-Othman, T S Sundareshan
• Prune belly appearance in a Turner subject. (1 February, 1986)

  A Savanelli, L Orfeo, M Stabile, S Iannuzzi, U De Bellis, G Esposito, V Ventruto