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Author/Creator Freedenberg, Debra

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. The association between newborn screening analytes and childhood autism in a Texas Medicaid population, 2010–2012. Issue 5 (24th April 2019)

Authors:
Canfield, Mark A.; Langlois, Peter H.; Rutenberg, Gary W.; Mandell, Dorothy J.; Hua, Fei; Reilly, Brendan; Ruktanonchai, Duke J.; Jackson, Janice F.; Hunt, Patricia; Freedenberg, Debra; Lee, Rachel; Villanacci, John F.
Journal:
American journal of medical genetics
Issue:
Volume 180:Issue 5(2019)
Page Start:
291
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. The association between newborn screening analytes as measured on a second screen and childhood autism in a Texas Medicaid population. Issue 6 (13th July 2020)

Authors:
Langlois, Peter H.; Canfield, Mark A.; Rutenberg, Gary W.; Mandell, Dorothy J.; Hua, Fei; Reilly, Brendan; Ruktanonchai, Duke J.; Jackson, Janice F.; Hunt, Patricia; Freedenberg, Debra; Lee, Rachel; Villanacci, John F.
Journal:
American journal of medical genetics
Issue:
Volume 183:Issue 6(2020)
Page Start:
331
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗