N R Dennis

Summary

Affiliation: University of Southampton
Country: UK

Publications

  1. ncbi A clinical, cytogenetic and molecular study of 47 females with r(X) chromosomes
    N Dennis
    Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK
    Ann Hum Genet 64:277-93. 2000
  2. ncbi Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13
    N R Dennis
    Division of Human Genetics, University of Southampton, Southampton, United Kingdom
    Am J Med Genet A 140:434-41. 2006
  3. ncbi Three patients with ring (X) chromosomes and a severe phenotype
    N R Dennis
    Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK
    J Med Genet 30:482-6. 1993
  4. ncbi The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders
    P F Bolton
    Section of Developmental Psychiatry, University of Cambridge, Cambridge, UK
    Am J Med Genet 105:675-85. 2001
  5. ncbi New case of "apple-peel" intestinal atresia and ocular anomalies with mosaic variegated aneuploidy
    K L Bower
    Am J Med Genet A 117:200-1. 2003
  6. ncbi A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype
    F Maggouta
    J Med Genet 40:e84. 2003
  7. ncbi Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays
    H Fiegler
    The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK
    J Med Genet 40:664-70. 2003
  8. ncbi The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes
    S M Gribble
    The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK
    J Med Genet 42:8-16. 2005

Collaborators

  • J A Crolla
  • A E Cockwell
  • John Ck Barber
  • S E Roberts
  • S M Gribble
  • H Fiegler
  • S Clegg
  • P Carr
  • K M Porter
  • N P Carter
  • E Prigmore
  • D C Burford
  • N S Thomas
  • K L Bower
  • F Maggouta
  • C E Browne
  • P Jacobs
  • P F Bolton
  • D Kalaitzopoulos
  • R Sandstrom
  • S A Youings
  • Bee Ling Ng
  • E J Douglas
  • I K Temple
  • P A Jacobs
  • C P R Williams
  • C Tyreman
  • P Hodgkins
  • M W M Veltman
  • D Wellesley
  • R J Thompson
  • M W Veltman

Detail Information

Publications8

  1. ncbi A clinical, cytogenetic and molecular study of 47 females with r(X) chromosomes
    N Dennis
    Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK
    Ann Hum Genet 64:277-93. 2000
    ..2. Thus some protection from oedema may be provided by the presence of two copies of Xq13.2...
  2. ncbi Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13
    N R Dennis
    Division of Human Genetics, University of Southampton, Southampton, United Kingdom
    Am J Med Genet A 140:434-41. 2006
    ..No correlations were found between specific clinical features and variations in breakpoints proximal and distal to the PWACR...
  3. ncbi Three patients with ring (X) chromosomes and a severe phenotype
    N R Dennis
    Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK
    J Med Genet 30:482-6. 1993
    ....
  4. ncbi The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders
    P F Bolton
    Section of Developmental Psychiatry, University of Cambridge, Cambridge, UK
    Am J Med Genet 105:675-85. 2001
    ..Further research will be required to clarify the range and basis of the phenotypic manifestations...
  5. ncbi New case of "apple-peel" intestinal atresia and ocular anomalies with mosaic variegated aneuploidy
    K L Bower
    Am J Med Genet A 117:200-1. 2003
  6. ncbi A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype
    F Maggouta
    J Med Genet 40:e84. 2003
  7. ncbi Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays
    H Fiegler
    The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK
    J Med Genet 40:664-70. 2003
    ....
  8. ncbi The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes
    S M Gribble
    The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK
    J Med Genet 42:8-16. 2005
    ....