Daniel H Williams

Summary

Publications

  1. ncbi request reprint Urorectal septum malformation sequence
    Daniel H Williams
    Department of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, USA
    Urology 66:657. 2005
  2. ncbi request reprint Prenatal diagnosis of Beckwith-Wiedemann syndrome
    Daniel H Williams
    Department of Urology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois 60614, USA
    Prenat Diagn 25:879-84. 2005
  3. ncbi request reprint Compound genetic abnormalities in patients with cystic fibrosis transmembrane regulator gene mutation
    Edward Karpman
    Scott Department of Urology, Baylor College of Medicine, Houston, Texas, USA
    Fertil Steril 87:1468.e5-8. 2007

Collaborators

  • Max Maizels
  • Edward Karpman
  • Larry I Lipshultz
  • Sidney Wilberforce

Detail Information

Publications3

  1. ncbi request reprint Urorectal septum malformation sequence
    Daniel H Williams
    Department of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, USA
    Urology 66:657. 2005
    ..Urologists should be familiar with the mechanisms and presentations of this condition, as they may be involved in the diagnosis and management of such patients...
  2. ncbi request reprint Prenatal diagnosis of Beckwith-Wiedemann syndrome
    Daniel H Williams
    Department of Urology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois 60614, USA
    Prenat Diagn 25:879-84. 2005
    ..To our knowledge, no established guidelines exist for the prenatal diagnosis of this condition. We present two new cases of prenatally diagnosed BWS and propose a diagnostic schema...
  3. ncbi request reprint Compound genetic abnormalities in patients with cystic fibrosis transmembrane regulator gene mutation
    Edward Karpman
    Scott Department of Urology, Baylor College of Medicine, Houston, Texas, USA
    Fertil Steril 87:1468.e5-8. 2007
    ..To determine the prevalence of compound genetic abnormalities in patients who are carriers of cystic fibrosis mutations...