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Author/Creator Hecht, Jacqueline T.

21. Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African‐American family. Issue 5 (7th May 2015)

Authors:
Cvjetkovic, Nevena; Maili, Lorena; Weymouth, Katelyn S.; Hashmi, S. Shahrukh; Mulliken, John B.; Topczewski, Jacek; Letra, Ariadne; Yuan, Qiuping; Blanton, Susan H.; Swindell, Eric C.; Hecht, Jacqueline T.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 3:Issue 5(2015:Sep.)
Page Start:
440
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

22. Role of WNT10A in failure of tooth development in humans and zebrafish. Issue 6 (14th September 2017)

Authors:
Yuan, Qiuping; Zhao, Min; Tandon, Bhavna; Maili, Lorena; Liu, Xiaoming; Zhang, Anqi; Baugh, Evan H.; Tran, Tam; Silva, Renato M.; Hecht, Jacqueline T.; Swindell, Eric C.; Wagner, Daniel S.; Letra, Ariadne
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 5:Issue 6(2017)
Page Start:
730
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

23. Soft tissue nasal asymmetry as an indicator of orofacial cleft predisposition. Issue 6 (16th April 2018)

Authors:
Zhang, Charles; Miller, Steven F.; Roosenboom, Jasmien; Wehby, George L.; Moreno Uribe, Lina M.; Hecht, Jacqueline T.; Deleyiannis, Frederic W. B.; Christensen, Kaare; Marazita, Mary L.; Weinberg, Seth M.
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 6(2018)
Page Start:
1296
Record Type:
Journal Article
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24. The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community. (November 2016)

Authors:
Weinberg, Seth M.; Raffensperger, Zachary D.; Kesterke, Matthew J.; Heike, Carrie L.; Cunningham, Michael L.; Hecht, Jacqueline T.; Kau, Chung How; Murray, Jeffrey C.; Wehby, George L.; Moreno, Lina M.; Marazita, Mary L.
Journal:
Cleft palate-craniofacial journal
Issue:
Volume 53:Number 6(2016)
Page Start:
185
Record Type:
Journal Article
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26. Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion. Issue 2 (February 2022)

Authors:
Quiggle, Ashley; Charng, Wu-Lin; Antunes, Lilian; Nikolov, Momchil; Bledsoe, Xavier; Hecht, Jacqueline T.; Dobbs, Matthew B.; Gurnett, Christina A.
Journal:
Clinical orthopaedics and related research
Issue:
Volume 480:Issue 2(2022)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗