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G W Hunter

Showing results (41-50 of 46) with videos related to

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Clinical Genetics|April 10, 2002
Participation rates of Ashkenazi Jews in a colon cancer community-based screening/prevention studyM Cappelli, A G W Hunter, H Stern, et al.
Human Genetics|October 18, 2002
A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolvedM Elizabeth McCready, Elizabeth Sweeney, Allan E Fryer, et al.
Human Molecular Genetics|June 19, 2003
Lathosterolosis: an inborn error of human and murine cholesterol synthesis due to lathosterol 5-desaturase deficiencyPatrycja A Krakowiak, Christopher A Wassif, Lisa Kratz, et al.
Journal of Breath Research|September 8, 2011
Smart sensor systems for human health breath monitoring applicationsG W Hunter, J C Xu, A M Biaggi-Labiosa, et al.
Journal of Medical Genetics|September 23, 2008
Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndromeM J Lyons, J M Graham, G Neri, et al.
Human Mutation|October 29, 2015
Mandibulofacial Dysostosis with Microcephaly: Mutation and Database UpdateLijia Huang, Megan R Vanstone, Taila Hartley, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Clinical Genetics|April 10, 2002
Participation rates of Ashkenazi Jews in a colon cancer community-based screening/prevention studyM Cappelli, A G W Hunter, H Stern, et al.
Human Genetics|October 18, 2002
A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolvedM Elizabeth McCready, Elizabeth Sweeney, Allan E Fryer, et al.
Human Molecular Genetics|June 19, 2003
Lathosterolosis: an inborn error of human and murine cholesterol synthesis due to lathosterol 5-desaturase deficiencyPatrycja A Krakowiak, Christopher A Wassif, Lisa Kratz, et al.
Journal of Breath Research|September 8, 2011
Smart sensor systems for human health breath monitoring applicationsG W Hunter, J C Xu, A M Biaggi-Labiosa, et al.
Journal of Medical Genetics|September 23, 2008
Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndromeM J Lyons, J M Graham, G Neri, et al.
Human Mutation|October 29, 2015
Mandibulofacial Dysostosis with Microcephaly: Mutation and Database UpdateLijia Huang, Megan R Vanstone, Taila Hartley, et al.
Pageof 5