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Author/Creator Oertel, Ralph

1. Characterization of core clinical phenotypes associated with recurrent proximal 15q25.2 microdeletions. Issue 1 (21st November 2013)

Authors:
Burgess, Trent; Brown, Natasha J.; Stark, Zornitza; Bruno, Damien L.; Oertel, Ralph; Chong, Belinda; Calabro, Vanessa; Kornberg, Andrew; Sanderson, Christine; Kelly, Julian; Howell, Katherine B.; Savarirayan, Ravi; Hinds, Rupert; Greenway, Anthea; Slater, Howard R.; White, Susan M.
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 1(2014.)
Page Start:
77
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Clinical audit of genetic testing and referral patterns for fragile X and associated conditions. Issue 6 (18th February 2016)

Authors:
Cotter, Megan; Archibald, Alison D.; McClaren, Belinda J.; Burgess, Trent; Francis, David; Hills, Louise; Martyn, Melissa; Oertel, Ralph; Slater, Howard; Cohen, Jonathan; Metcalfe, Sylvia A.
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 6(2016)
Page Start:
1439
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. FMR1 allele size distribution in 35, 000 males and females: a comparison of developmental delay and general population cohorts. (December 2018)

Authors:
Kraan, Claudine; Bui, Quang; Field, Mike; Archibald, Alison; Metcalfe, Sylvia; Christie, Louise; Bennetts, Bruce; Oertel, Ralph; Smith, Melanie; du Sart, Desiree; Bruno, Damien; Wotton, Tiffany; Amor, David; Francis, David; Godler, David
Journal:
Genetics in medicine
Issue:
Volume 20:Number 12(2018)
Page Start:
1627
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Lessons learnt from multifaceted diagnostic approaches to the first 150 families in Victoria's Undiagnosed Diseases Program. Issue 8 (5th November 2021)

Authors:
Cloney, Thomas; Gallacher, Lyndon; Pais, Lynn S; Tan, Natalie B; Yeung, Alison; Stark, Zornitza; Brown, Natasha J; McGillivray, George; Delatycki, Martin B; de Silva, Michelle G; Downie, Lilian; Stutterd, Chloe A; Elliott, Justine; Compton, Alison G; Lovgren, Alysia; Oertel, Ralph; Francis, David...
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 8(2022)
Page Start:
748
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗