Table of contents

Research Article

• Osteogenesis imperfecta type IIA: evidence for dominant inheritance. (1 July, 1987)

  I D Young, E M Thompson, C M Hall, M E Pembrey
• Recurrence risks and prognosis in severe sporadic osteogenesis imperfecta. (1 July, 1987)

  E M Thompson, I D Young, C M Hall, M E Pembrey
• Prenatal prediction of osteogenesis imperfecta (OI type IV): exclusion of inheritance using a collagen gene probe. (1 July, 1987)

  P Tsipouras, R C Schwartz, J D Goldberg, R L Berkowitz, F Ramirez
• Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4. (1 July, 1987)

  C McKeown, A P Read, A Dodge, O Stecko, A Mercer, R Harris
• The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27. (1 July, 1987)

  H Veenema, N J Carpenter, E Bakker, M H Hofker, A M Ward, P L Pearson
• Postaxial acrofacial dysostosis (Miller) syndrome. (1 July, 1987)

  D Donnai, H E Hughes, R M Winter
• 18q-syndrome and extraskeletal Ewing's sarcoma. (1 July, 1987)

  M Machin Valtueña, J M Garcia-Sagredo, A Muñoz Villa, C Lozano Giménez, J M Aparicio Meix
• An isodicentric X chromosome with short arm fusion in a woman without somatic features of Turner's syndrome. (1 July, 1987)

  I C Barnes, D J Curtis, S L Duncan
• Translocation X;13 in a patient with retinoblastoma. (1 July, 1987)

  G Ponzio, E Savin, G Cattaneo, M P Ghiotti, A Marra, O Zuffardi, C Danesino
• Partial monosomy 12p13.1----13.3. (1 July, 1987)

  D R Romain, J Goldsmith, L M Columbano-Green, C J Chapman, R H Smythe, R G Parfitt
• De novo 2q+ masquerading as Smith-Lemli-Opitz syndrome. (1 July, 1987)

  A E Donnenfeld, E H Zackai, D M McDonald, R Aquino, B S Emanuel
• Incontinentia pigmenti in a boy with Klinefelter's syndrome. (1 July, 1987)

  A D Ormerod, M I White, E McKay, A W Johnston