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I Markowitz

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American Journal of Medical Genetics|October 23, 1997
Skeletal anomalies and deformities in patients with deletions of 22q11J E Ming, D M McDonald-McGinn, T E Megerian, et al.
American Journal of Human Genetics|March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeM Muenke, K W Gripp, D M McDonald-McGinn, et al.
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Showing results (111-120 of 112) with videos related to

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You have reached the last page of results.This site can display upto 112 results.
American Journal of Medical Genetics|October 23, 1997
Skeletal anomalies and deformities in patients with deletions of 22q11J E Ming, D M McDonald-McGinn, T E Megerian, et al.
American Journal of Human Genetics|March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeM Muenke, K W Gripp, D M McDonald-McGinn, et al.
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