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Author/Creator Sund, Sarah

1. A Prospective, Crossover Survey Study of Child- and Proxy-Reported Quality of Life According to Spinal Muscular Atrophy Type and Medical Interventions. (April 2020)

Authors:
Weaver, Meaghann S.; Hanna, Rewais; Hetzel, Scott; Patterson, Karen; Yuroff, Alice; Sund, Sarah; Schultz, Meredith; Schroth, Mary; Halanski, Matthew A.
Journal:
Journal of child neurology
Issue:
Volume 35:Number 5(2020:May)
Page Start:
322
Record Type:
Journal Article
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3. KIAA1217: A novel candidate gene associated with isolated and syndromic vertebral malformations. Issue 7 (5th May 2020)

Authors:
Al Dhaheri, Noura; Wu, Nan; Zhao, Sen; Wu, Zhihong; Blank, Robert D.; Zhang, Jianguo; Raggio, Cathy; Halanski, Matthew; Shen, Jianxiong; Noonan, Ken; Qiu, Guixing; Nemeth, Blaise; Sund, Sarah; Dunwoodie, Sally L.; Chapman, Gavin; Glurich, Ingrid; Steiner, Robert D.; Wohler, Elizabeth; Martin, Ren...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 7(2020)
Page Start:
1664
Record Type:
Journal Article
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4. Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel–Feil and Treacher Collins syndromes. (27th October 2014)

Authors:
Giampietro, Philip F.; Armstrong, Linlea; Stoddard, Alex; Blank, Robert D.; Livingston, Janet; Raggio, Cathy L.; Rasmussen, Kristen; Pickart, Michael; Lorier, Rachel; Turner, Amy; Sund, Sarah; Sobrera, Nara; Neptune, Enid; Sweetser, David; Santiago‐Cornier, Alberto; Broeckel, Ulrich
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 1(2015:Jan.)
Page Start:
95
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗