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J Mackenzie

Showing results (721-730 of 725) with videos related to

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Journal of Medicinal Chemistry|December 21, 2018
Identification of GSK3186899/DDD853651 as a Preclinical Development Candidate for the Treatment of Visceral LeishmaniasisMichael G Thomas, Manu De Rycker, Myriam Ajakane, et al.
JAMA Surgery|December 20, 2018
Association Between 6-Week Postdischarge Risk Classification and 12-Month Outcomes After Orthopedic TraumaRenan C Castillo, Yanjie Huang, Daniel Scharfstein, et al.
Nature Genetics|July 2, 2021
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndromeMargot A Cousin, Blake A Creighton, Keith A Breau, et al.
Human Reproduction (Oxford, England)|November 30, 2020
Top 10 priorities for future infertility research: an international consensus development study†  ‡J M N Duffy, G D Adamson, E Benson, et al.
American Journal of Human Genetics|February 17, 2021
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in femalesFrancesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, et al.
Pageof 73

Showing results (721-730 of 725) with videos related to

Sort By:
Pageof 73
You have reached the last page of results.This site can display upto 725 results.
Journal of Medicinal Chemistry|December 21, 2018
Identification of GSK3186899/DDD853651 as a Preclinical Development Candidate for the Treatment of Visceral LeishmaniasisMichael G Thomas, Manu De Rycker, Myriam Ajakane, et al.
JAMA Surgery|December 20, 2018
Association Between 6-Week Postdischarge Risk Classification and 12-Month Outcomes After Orthopedic TraumaRenan C Castillo, Yanjie Huang, Daniel Scharfstein, et al.
Nature Genetics|July 2, 2021
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndromeMargot A Cousin, Blake A Creighton, Keith A Breau, et al.
Human Reproduction (Oxford, England)|November 30, 2020
Top 10 priorities for future infertility research: an international consensus development study†  ‡J M N Duffy, G D Adamson, E Benson, et al.
American Journal of Human Genetics|February 17, 2021
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in femalesFrancesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, et al.
Pageof 73