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Author/Creator Bethune, M.

2. OC06.04: Population‐based prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort. (30th September 2019)

Authors:
Hui, L.; Poulton, A.; Kluckow, E.; Lindquist, A.; Hutchinson, B.; Pertile, M.D.; Bonacquisto, L.; Gugasyan, L.; Kulkarni, A.; Harraway, J.; Howden, A.; McCoy, R.; da Silva Costa, F.; Menezes, M.; Palma‐Dias, R.; Nisbet, D.; Martin, N.; Bethune, M.; Poulakis, Z.; Halliday, J.
Journal:
Ultrasound in obstetrics & gynecology
Issue:
Volume 54(2019)Supplement 1
Page Start:
14
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. State-Wide Utilization and Performance of Traditional and Cell-Free DNA-Based Prenatal Testing Pathways: The Victorian Perinatal Record Linkage (PeRL) Study. Issue 1 (January 2021)

Authors:
Lindquist, A.; Hui, L.; Poulton, A.; Kluckow, E.; Hutchinson, B.; Pertile, M. D.; Bonacquisto, L.; Gugasyan, L.; Kulkarni, A.; Harraway, J.; Howden, A.; McCoy, R.; da Silva Costa, F.; Menezes, M.; Palma-Dias, R.; Nisbet, D.; Martin, N.; Bethune, M.; Poulakis, Z.; Halliday, J.
Journal:
Obstetrical & gynecological survey
Issue:
Volume 76:Issue 1(2021)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. State‐wide utilization and performance of traditional and cell‐free DNA‐based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study. (1st August 2020)

Authors:
Lindquist, A.; Hui, L.; Poulton, A.; Kluckow, E.; Hutchinson, B.; Pertile, M. D.; Bonacquisto, L.; Gugasyan, L.; Kulkarni, A.; Harraway, J.; Howden, A.; McCoy, R.; Da Silva Costa, F.; Menezes, M.; Palma‐Dias, R.; Nisbet, D.; Martin, N.; Bethune, M.; Poulakis, Z.; Halliday, J.
Journal:
Ultrasound in obstetrics & gynecology
Issue:
Volume 56:Number 2(2020)
Page Start:
215
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗