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American Journal of Human Genetics
|
May 29, 2018
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3
Sophia R Cameron-Christie, Constance F Wells, Marleen Simon, et al.
Arthritis Care & Research
|
March 2, 2010
Self-directed learning of basic musculoskeletal ultrasound among rheumatologists in the United States
Eugene Y Kissin, Jane Nishio, Mei Yang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 30, 2023
Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities
Marcello Scala, Kamal Khan, Claire Beneteau, et al.
Molecular Psychiatry
|
February 7, 2025
βIV spectrin abundancy, cellular distribution and sensitivity to AKT/GSK3 regulation in schizophrenia
Jessica Di Re, Michela Marini, Syed Ibrar Hussain, et al.
Cell Stem Cell
|
February 16, 2023
Natural variation in gene expression and viral susceptibility revealed by neural progenitor cell villages
Michael F Wells, James Nemesh, Sulagna Ghosh, et al.
Marine Pollution Bulletin
|
May 30, 2020
Sediment metal enrichment and ecological risk assessment of ten ports and estuaries in the World Harbours Project
G F Birch, J-H Lee, E Tanner, et al.
Nature Communications
|
April 29, 2025
Global diversity and distribution of antibiotic resistance genes in human wastewater treatment systems
Congmin Zhu, Linwei Wu, Daliang Ning, et al.
Nature Microbiology
|
November 16, 2019
Author Correction: Global diversity and biogeography of bacterial communities in wastewater treatment plants
Linwei Wu, Daliang Ning, Bing Zhang, et al.
Nature Microbiology
|
May 16, 2019
Global diversity and biogeography of bacterial communities in wastewater treatment plants
Linwei Wu, Daliang Ning, Bing Zhang, et al.
HGG Advances
|
July 9, 2026
ALG14 Variants Contribute to a Congenital Disorder of Glycosylation Characterized by Congenital Myasthenia and Epilepsy
Jonathan Marquez, Flavien Rouxel, Fatima E It, et al.
Page
of 24
Search research articles
Search
Showing results (221-230 of 233) with videos related to
Sort By:
Page
of 24
American Journal of Human Genetics
|
May 29, 2018
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3
Sophia R Cameron-Christie, Constance F Wells, Marleen Simon, et al.
Arthritis Care & Research
|
March 2, 2010
Self-directed learning of basic musculoskeletal ultrasound among rheumatologists in the United States
Eugene Y Kissin, Jane Nishio, Mei Yang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 30, 2023
Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities
Marcello Scala, Kamal Khan, Claire Beneteau, et al.
Molecular Psychiatry
|
February 7, 2025
βIV spectrin abundancy, cellular distribution and sensitivity to AKT/GSK3 regulation in schizophrenia
Jessica Di Re, Michela Marini, Syed Ibrar Hussain, et al.
Cell Stem Cell
|
February 16, 2023
Natural variation in gene expression and viral susceptibility revealed by neural progenitor cell villages
Michael F Wells, James Nemesh, Sulagna Ghosh, et al.
Marine Pollution Bulletin
|
May 30, 2020
Sediment metal enrichment and ecological risk assessment of ten ports and estuaries in the World Harbours Project
G F Birch, J-H Lee, E Tanner, et al.
Nature Communications
|
April 29, 2025
Global diversity and distribution of antibiotic resistance genes in human wastewater treatment systems
Congmin Zhu, Linwei Wu, Daliang Ning, et al.
Nature Microbiology
|
November 16, 2019
Author Correction: Global diversity and biogeography of bacterial communities in wastewater treatment plants
Linwei Wu, Daliang Ning, Bing Zhang, et al.
Nature Microbiology
|
May 16, 2019
Global diversity and biogeography of bacterial communities in wastewater treatment plants
Linwei Wu, Daliang Ning, Bing Zhang, et al.
HGG Advances
|
July 9, 2026
ALG14 Variants Contribute to a Congenital Disorder of Glycosylation Characterized by Congenital Myasthenia and Epilepsy
Jonathan Marquez, Flavien Rouxel, Fatima E It, et al.
Page
of 24