Dr Lisa Ewans

Clinical Associate Lecturer
Genetic Medicine
Royal Prince Alfred Hospital

Telephone 9515 5080
Fax 9515 5082

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Selected publications

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Journals

  • Eggers, S., Sadedin, S., van den Bergen, J., Robevska, G., Ohnesorg, T., Hewitt, J., Lambeth, L., Smith, G., Smith, J., Ewans, L., Shalhoub, C., Cowell, C., et al (2016). Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort. Genome Biology, 17(1), 1-21. [More Information]
  • Jedraszak, G., Demeer, B., Mathieu-Dramard, M., Andrieux, J., Receveur, A., Weber, A., Maye, U., Foulds, N., Temple, I., Crolla, J., Ewans, L., Wilson, M., et al (2015). Clinical and Molecular Characterization of the 20q11.2 Microdeletion Syndrome: Six New Patients. American Journal of Medical Genetics. Part A, 167A (3), 504-511. [More Information]

2016

  • Eggers, S., Sadedin, S., van den Bergen, J., Robevska, G., Ohnesorg, T., Hewitt, J., Lambeth, L., Smith, G., Smith, J., Ewans, L., Shalhoub, C., Cowell, C., et al (2016). Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort. Genome Biology, 17(1), 1-21. [More Information]

2015

  • Jedraszak, G., Demeer, B., Mathieu-Dramard, M., Andrieux, J., Receveur, A., Weber, A., Maye, U., Foulds, N., Temple, I., Crolla, J., Ewans, L., Wilson, M., et al (2015). Clinical and Molecular Characterization of the 20q11.2 Microdeletion Syndrome: Six New Patients. American Journal of Medical Genetics. Part A, 167A (3), 504-511. [More Information]

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