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Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity
2010
241 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
11.49
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity | Researchclopedia
Pamela J. Reitnauer
·
Cone Health
Rosemarie Smith
·
Maine Medical Center
David W. Stockton
·
Wayne State University
Hiltrud Muhle
·
Christian-Albrechts-Universität zu Kiel
Ingo Helbig
·
Christian-Albrechts-Universität zu Kiel
Evan E. Eichler
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University of Washington
Blake C. Ballif
·
Signature Research (United States)
Jill A. Rosenfeld
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Signature Research (United States)
Karen D. Tsuchiya
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Seattle Children's Hospital