Table of contents

Research Article

• Confined placental mosaicism. (1 July, 1996)

  D K Kalousek, M Vekemans
• Increased incidence of cancer in first degree relatives of women with double primary carcinomas of the breast and colon. (1 July, 1996)

  W D Foulkes, N Bolduc, D Lambert, O Ginsburg, L Olien, D W Yandell, P N Tonin, S A Narod
• Attitudes to predictive DNA testing in familial adenomatous polyposis. (1 July, 1996)

  S Whitelaw, J M Northover, S V Hodgson
• Attitudes towards bipolar disorder and predictive genetic testing among patients and providers. (1 July, 1996)

  L B Smith, B Sapers, V I Reus, N B Freimer
• Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis. (1 July, 1996)

  S C Yau, M Bobrow, C G Mathew, S J Abbs
• Report of a critical recombination further narrowing the TSC1 region. (1 July, 1996)

  K S Au, J Murrell, A Buckler, S H Blanton, H Northrup
• Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH. (1 July, 1996)

  J J Engelen, W J Loots, J C Albrechts, P C Motoh, J P Fryns, A J Hamers, J P Geraedts
• Evidence of a long QT founder gene with varying phenotypic expression in South African families. (1 July, 1996)

  T de Jager, C H Corbett, J C Badenhorst, P A Brink, V A Corfield
• Down syndrome in association with features of the androgen insensitivity syndrome. (1 July, 1996)

  R M Viner, N Shimura, B D Brown, A J Green, I A Hughes
• Holoprosencephaly in the west of Scotland 1975-1994. (1 July, 1996)

  M L Whiteford, J L Tolmie
• Pallister-Hall syndrome. (1 July, 1996)

  L G Biesecker, J M Graham
• Linkage disequilibrium between four intragenic polymorphic microsatellites of the NF1 gene and its implications for genetic counselling. (1 July, 1996)

  M C Valero, E Velasco, A Valero, F Moreno, C Hernández-Chico
• An autosomal dominant syndrome of renal and anogenital malformations with syndactyly. (1 July, 1996)

  A J Green, R N Sandford, B C Davison
• Possible autosomal recessive inheritance of progressive hearing loss with stapes fixation. (1 July, 1996)

  C Thies, M Handrock, K Sperling, A Rcis
• A case of duplication of 13q32-->qter and deletion of 18p11.32-->pter with mild phenotype: Patau syndrome and duplications of 13q revisited. (1 July, 1996)

  N Helali, A K Iafolla, S G Kahler, M B Qumsiyeh
• Prenatal diagnosis in Treacher Collins syndrome using combined linkage analysis and ultrasound imaging. (1 July, 1996)

  S J Edwards, A Fowlie, M P Cust, D T Liu, I D Young, M J Dixon
• Xeroderma pigmentosum--Cockayne syndrome complex: a further case. (1 July, 1996)

  B C Hamel, A Raams, A R Schuitema-Dijkstra, P Simons, I van der Burgt, N G Jaspers, W J Kleijer
• FRAXF in a patient with chromosome 8 duplication. (1 July, 1996)

  A M Vianna-Morgante, R C Mingroni-Netto, A C Barbosa, P A Otto, C Rosenberg
• Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation. (1 July, 1996)

  C P Chen, F F Liu, S W Jan, C P Chen, C C Lan
• MURCS association: case report and review. (1 July, 1996)

  C Braun-Quentin, C Billes, B Böwing, D Kotzot
• Nephropathy and growth hormone deficiency in a patient with mitochondrial tRNA(Leu(UUR)) mutation. (1 July, 1996)

  T Yorifuji, M Kawai, T Momoi, H Sasaki, K Furusho, J Muroi, K Shimizu, Y Takahashi, M Matsumura, M Nambu, T Okuno
• An ovine CFTR variant as a putative cystic fibrosis causing mutation. (1 July, 1996)

  S J Tebbutt, A Harris, D F Hill
• A mild phenotype associated with der(9)t(3;9) (p25;p23). (1 July, 1996)

  R J McClure, N Telford, S J Newell
• Still no evidence for heterogeneity in Best's vitelliform macular dystrophy. (1 July, 1996)

  C Graff, C Wadelius