Table of contents

Research Article

• Marfan syndrome: a mystery solved. (1 February, 1992)

  P Tsipouras
• A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium study. (1 February, 1992)

  M Sarfarazi, P Tsipouras, R Del Mastro, M Kilpatrick, P Farndon, M Boxer, A Bridges, C Boileau, C Junien, C Hayward
• Marfan syndrome in a large family: response of family members to a screening programme. (1 February, 1992)

  A B Bridges, M Faed, M Boxer, J R Gray, C Bundy, A Murray
• Sensorineural deafness inherited as a tissue specific mitochondrial disorder. (1 February, 1992)

  L Jaber, M Shohat, X Bu, N Fischel-Ghodsian, H Y Yang, S J Wang, J I Rotter
• Fetal hydrops. (1 February, 1992)

  P A Boyd, J W Keeling
• Chromosome in situ suppression hybridisation in human male meiosis. (1 February, 1992)

  A S Goldman, M A Hultén
• Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding. (1 February, 1992)

  P A Jacobs, C Browne, N Gregson, C Joyce, H White
• Cyclophosphamide increases the frequency of sister chromatid exchange in direct preparations of human chorionic villi in the absence of supplementary enzymatic activation systems. (1 February, 1992)

  S Pariani, M Buscaglia, M Piantanida, G Simoni
• The clinicopathological features of three babies with osteogenesis imperfecta resulting from the substitution of glycine by valine in the pro alpha 1 (I) chain of type I procollagen. (1 February, 1992)

  W G Cole, E Patterson, J Bonadio, P E Campbell, D W Fortune
• The lipoprotein lipase Gly188----Glu mutation in South Africans of Indian descent: evidence suggesting common origins and an increased frequency. (1 February, 1992)

  H E Henderson, F Hassan, G M Berger, M R Hayden
• Multiple mutation in an extended Duchenne muscular dystrophy family. (1 February, 1992)

  A Miciak, A Keen, D Jadayel, S Bundey
• Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients. (1 February, 1992)

  L Vitiello, M L Mostacciuolo, S Oliviero, F Schiavon, L Nicoletti, C Angelini, G A Danieli
• Cystic fibrosis mutations delta F508 and G542X in Jewish patients. (1 February, 1992)

  I Lerer, M Sagi, G R Cutting, D Abeliovich
• Recurrence of neural tube defect in a group of at risk women: a 10 year study of Pregnavite Forte F. (1 February, 1992)

  M Holmes-Siedle, R H Lindenbaum, A Galliard
• Unusual T cell clones in a patient with Nijmegen breakage syndrome. (1 February, 1992)

  D Stoppa-Lyonnet, D Girault, F LeDeist, A Aurias
• Sociocultural problems in genetic counselling. (1 February, 1992)

  M Naveed, S R Phadke, A Sharma, S S Agarwal
• Meckel syndrome and neural tube defects in Kuwait. (1 February, 1992)

  A S Teebi, Q A al Saleh, H Odeh
• Fertility in a male with trisomy 21. (1 February, 1992)

  M Bobrow, T Barby, A Hajianpour, D Maxwell, S C Yau
• Maxillonasal dysplasia (Binder's syndrome) and chondrodysplasia punctata. (1 February, 1992)

  F Serville