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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 Leishmaniasis
Michael 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 Trauma
Renan C Castillo, Yanjie Huang, Daniel Scharfstein, et al.
Nature Genetics
|
July 2, 2021
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome
Margot 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 females
Francesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, et al.
Page
of 73
Search research articles
Search
Showing results (721-730 of 725) with videos related to
Sort By:
Page
of 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 Leishmaniasis
Michael 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 Trauma
Renan C Castillo, Yanjie Huang, Daniel Scharfstein, et al.
Nature Genetics
|
July 2, 2021
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome
Margot 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 females
Francesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, et al.
Page
of 73