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Author/Creator Roeder, Elizabeth R

1. Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond–Blackfan anaemia. Issue 11 (4th October 2010)

Authors:
Wat, Margaret J; Enciso, Victoria B; Wiszniewski, Wojciech; Resnick, Trevor; Bader, Patricia; Roeder, Elizabeth R; Freedenberg, Debra; Brown, Chester; Stankiewicz, Pawel; Cheung, Sau-Wai; Scott, Daryl A
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 11(2010)
Page Start:
777
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size. Issue 5 (12th November 2009)

Authors:
Shinawi, Marwan; Liu, Pengfei; Kang, Sung-Hae L; Shen, Joseph; Belmont, John W; Scott, Daryl A; Probst, Frank J; Craigen, William J; Graham, Brett H; Pursley, Amber; Clark, Gary; Lee, Jennifer; Proud, Monica; Stocco, Amber; Rodriguez, Diana L; Kozel, Beth A; Sparagana, Steven; Roeder, Elizabeth R...
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 5(2010)
Page Start:
332
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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