Table of contents

Research Article

• Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females. (1 April, 1992)

  C Moutou, C Junien, I Henry, C Bonaïti-Pellié
• Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome. (1 April, 1992)

  D Viljoen, R Ramesar
• Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation. (1 April, 1992)

  T Ogata, J R Hawkins, A Taylor, N Matsuo, J Hata, P N Goodfellow
• Highly polymorphic XbaI RFLPs of the human 21-hydroxylase genes among Chinese. (1 April, 1992)

  L Chen, X Pan, Y Shen, Z Chen, Y Zhang, R Chen
• Screening of microdeletions of chromosome 20 in patients with Alagille syndrome. (1 April, 1992)

  C Desmaze, J F Deleuze, A M Dutrillaux, G Thomas, M Hadchouel, A Aurias
• Confirmation of genetic linkage between atopic IgE responses and chromosome 11q13. (1 April, 1992)

  R P Young, P A Sharp, J R Lynch, J A Faux, G M Lathrop, W O Cookson, J M Hopkin
• Age at onset and life table risks in genetic counselling for Huntington's disease. (1 April, 1992)

  P S Harper, R G Newcombe
• Genetic and clinical studies in autosomal dominant polycystic kidney disease type 1 (ADPKD1). (1 April, 1992)

  E Coto, S Aguado, J Alvarez, M J Menéndez Díaz, C López-Larrea
• Evidence for linkage disequilibrium between D16S94 and the adult onset polycystic kidney disease (PKD1) gene. (1 April, 1992)

  S E Pound, A D Carothers, P M Pignatelli, A M Macnicol, M L Watson, A F Wright
• A strategy for the rapid isolation of new PCR based DNA polymorphisms. (1 April, 1992)

  P R Hoban, M F Santibanez-Koref, J Heighway
• Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation. (1 April, 1992)

  I D Young, J M Zuccollo, E L Maltby, N J Broderick
• A complex chromosome rearrangement with 10 breakpoints: tentative assignment of the locus for Williams syndrome to 4q33----q35.1. (1 April, 1992)

  R Tupler, P Maraschio, A Gerardo, R Mainieri, G Lanzi, L Tiepolo
• Evidence that Rieger syndrome maps to 4q25 or 4q27. (1 April, 1992)

  C Vaux, L Sheffield, C G Keith, L Voullaire
• Interstitial deletion of the distal long arm of chromosome 4. (1 April, 1992)

  P Sarda, G Lefort, J P Fryns, C Humeau, D Rieu
• The orocraniodigital syndrome of Juberg and Hayward. (1 April, 1992)

  A Verloes, M Le Merrer, J C Davin, P Wittamer, C Abrassart, G Bricteux, M L Briard
• The Baller-Gerold syndrome. (1 April, 1992)

  L Van Maldergem, A Verloes, L Lejeune, Y Gillerot
• Postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation: a new syndrome? (1 April, 1992)

  K Zerres, M Rietschel, E Rietschel, F Majewski, P Meinecke
• Hypoglossia-hypodactyly syndrome with hydrocephalus. (1 April, 1992)

  A H Lipson, D D Weaver
• Fragile X syndrome: as common as first thought? (1 April, 1992)

  R D Smart