H Bruyere

Summary

Affiliation: University of British Columbia
Country: Canada

Publications

  1. ncbi Isodicentric Yp: prenatal diagnosis and outcome in 12 cases
    H Bruyere
    Department of Pathology and Laboratory Medicine, Vancouver University of British Columbia, Vancouver, BC, Canada
    Prenat Diagn 26:324-9. 2006
  2. ncbi Concomitant and successive amplifications of MYC in APL-like leukemia
    Helene Bruyere
    Department of Pathology and Laboratory Medicine, Vancouver General Hospital and University of British Columbia, Vancouver, BC, Canada
    Cancer Genet Cytogenet 197:75-80. 2010
  3. ncbi V37I connexin 26 allele in patients with sensorineural hearing loss: evidence of its pathogenicity
    C Huculak
    Department of Medical Genetics, University of British Columbia, Vancouver, Canada
    Am J Med Genet A 140:2394-400. 2006
  4. ncbi Risk of mosaicism and uniparental disomy associated with the prenatal diagnosis of a non-homologous Robertsonian translocation carrier
    H Bruyere
    Department of Pathology, University of British Columbia, Vancouver, B C, Canada
    Fetal Diagn Ther 19:399-403. 2004
  5. ncbi Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI: case report
    S Ma
    Department of Obstetrics and Gynecology, University of British Columbia, Vancouver, BC, Canada
    Hum Reprod 18:2298-301. 2003

Collaborators

Detail Information

Publications5

  1. ncbi Isodicentric Yp: prenatal diagnosis and outcome in 12 cases
    H Bruyere
    Department of Pathology and Laboratory Medicine, Vancouver University of British Columbia, Vancouver, BC, Canada
    Prenat Diagn 26:324-9. 2006
    ..2. To review the literature and provide recommendations for cytogenetic analysis and counseling...
  2. ncbi Concomitant and successive amplifications of MYC in APL-like leukemia
    Helene Bruyere
    Department of Pathology and Laboratory Medicine, Vancouver General Hospital and University of British Columbia, Vancouver, BC, Canada
    Cancer Genet Cytogenet 197:75-80. 2010
    ..This report presents a second patient with APL-like bone marrow morphology, absence of RARA rearrangement, and MYC amplification. In this case, the amplification happened in various concomitant or successive forms...
  3. ncbi V37I connexin 26 allele in patients with sensorineural hearing loss: evidence of its pathogenicity
    C Huculak
    Department of Medical Genetics, University of British Columbia, Vancouver, Canada
    Am J Med Genet A 140:2394-400. 2006
    ....
  4. ncbi Risk of mosaicism and uniparental disomy associated with the prenatal diagnosis of a non-homologous Robertsonian translocation carrier
    H Bruyere
    Department of Pathology, University of British Columbia, Vancouver, B C, Canada
    Fetal Diagn Ther 19:399-403. 2004
    ..To estimate the fetal risk of uniparental disomy (UPD) associated with the presence of a Robertsonian translocation (RT) in a parent or in the fetus, to determine whether it is clinically indicated to test these pregnancies for UPD...
  5. ncbi Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI: case report
    S Ma
    Department of Obstetrics and Gynecology, University of British Columbia, Vancouver, BC, Canada
    Hum Reprod 18:2298-301. 2003
    ..The molecular and cytogenetic studies indicated a 46,XX male infant without the SRY gene or 46,XX/XY mosaicism. The possible mechanism in this SRY-negative XX male by ICSI is discussed...