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Author/Creator Blank, Robert D.

2. 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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3. Muscle Strength and Physical Performance Are Associated With Risk of Postfracture Mortality But Not Subsequent Fracture in Men. (6th July 2022)

Authors:
Alajlouni, Dima A.; Bliuc, Dana; Tran, Thach S.; Blank, Robert D.; Cawthon, Peggy M.; Ensrud, Kristine E.; Lane, Nancy E.; Orwoll, Eric S.; Cauley, Jane A.; Center, Jacqueline R.
Journal:
Journal of bone and mineral research
Issue:
Volume 37:Number 8(2022)
Page Start:
1571
Record Type:
Journal Article
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4. Secondary Fracture Prevention: Consensus Clinical Recommendations From a Multistakeholder Coalition. (May 2020)

Authors:
Conley, Robert B.; Adib, Gemma; Adler, Robert A.; Åkesson, Kristina E.; Alexander, Ivy M.; Amenta, Kelly C.; Blank, Robert D.; Brox, William Timothy; Carmody, Emily E.; Chapman-Novakofski, Karen; Clarke, Bart L.; Cody, Kathleen M.; Cooper, Cyrus; Crandall, Carolyn J.; Dirschl, Douglas R.; Eagen, ...
Journal:
Orthopedic nursing
Issue:
Volume 39:Number 3(2020)
Page Start:
Record Type:
Journal Article
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5. 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) ↗